55615288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72823744-T-G

http://identifiers.org/hco/15/GRCh38#55615347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72823684-A-C

55615357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72823674-T-C

55615762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72823308-G-T

55615896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72823162-G-C

55615937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72823129-C-G

55615947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72823119-A-G

55616003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72823060-T-C

55616196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72822965-G-C

55616229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72822934-G-A

55616393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72822845-G-A

55616393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72822845-G-T

55616419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72822819-A-T

55616456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72822780-C-T

55616494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72822750-G-A

http://identifiers.org/hco/15/GRCh38#55616551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72822692-C-A

http://identifiers.org/hco/15/GRCh38#55616980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72822258-C-A

55616980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72822258-C-T

55617188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72822049-A-T

http://identifiers.org/hco/15/GRCh38#55617484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72821766-C-A

55617710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72821575-A-G

55617710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72821575-A-T

55617724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72821563-T-C

55618041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72821271-G-T

55618262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72821050-T-C

55618326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72821015-G-T

55618545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72820781-G-T

http://identifiers.org/hco/15/GRCh38#55618681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72820699-C-A

55618747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72820649-G-T

55618937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72820459-T-C

http://identifiers.org/hco/15/GRCh38#55618953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72820443-C-A

55619078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72820321-A-G

55619100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72820303-G-T

55619112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72820291-G-A

55619112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72820291-G-T

55619121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72820282-C-G

55619121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72820282-C-T

55619381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72820056-G-T

55619463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72819985-T-C

55619463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72819985-T-G

http://identifiers.org/hco/15/GRCh38#55619846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72819597-C-A

55619846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72819597-C-T

55619873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72819570-A-G

55619910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72819536-T-C

http://identifiers.org/hco/15/GRCh38#55619977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72819475-C-A

55619977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72819475-C-T

55619994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72819458-T-A

55619994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3 prime UTR variant
orthologous variants: 72819458-T-C

55620160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72819290-G-A

55620500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72818164-C-G

55620509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72818154-C-T

55620522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72818137-G-T

55620537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72818124-A-T

55621921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72817214-G-A

55621923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72817212-A-G

55624413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72815075-G-C

55624431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72815057-T-C

http://identifiers.org/hco/15/GRCh38#55624451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72815037-C-A

55624453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: synonymous variant
orthologous variants: 72815035-G-A

http://identifiers.org/hco/15/GRCh38#55624457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72815031-C-A

55624457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72815031-C-T

55624481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72815007-T-C

55624481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72815007-T-G

http://identifiers.org/hco/15/GRCh38#55624617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72814469-C-A

55624617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72814469-C-T

55624644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72814442-T-A

55624644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72814442-T-G

55627148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72813409-T-C

55627154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72813403-G-C

55627154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72813403-G-T

http://identifiers.org/hco/15/GRCh38#55627159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72813398-A-C

55627159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72813398-A-G

http://identifiers.org/hco/15/GRCh38#55627259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72813312-A-C

http://identifiers.org/hco/15/GRCh38#55627272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72813299-C-A

55627276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72813295-G-A

55627276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72813295-G-T

55627285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72813285-A-T

55627517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72813180-T-C

55627517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72813180-T-G

55627538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72813154-C-T

55627622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72813093-G-A

55627645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72813076-T-C

55627660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72813061-G-T

55627852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812955-G-A

55627986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812837-G-C

55628137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812717-C-T

55628315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812599-G-C

55628329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812585-T-C

55628559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812392-T-C

55628728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812242-T-C

55628731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812239-G-T

55628744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812226-G-A

55628744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812226-G-T

http://identifiers.org/hco/15/GRCh38#55628751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72812219-C-A

55628751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812219-C-G

55628751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812219-C-T

55628801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812188-T-C

55628808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812181-G-A

55628808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812181-G-C

55628808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812181-G-T

http://identifiers.org/hco/15/GRCh38#55628810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72812179-C-A

55628810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72812179-C-T

http://identifiers.org/hco/15/GRCh38#55629144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72811882-A-C

55629385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72811278-G-A

55629385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72811278-G-T

55631045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, missense_variant
orthologous variants: 72809507-G-A

55631045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, missense_variant
orthologous variants: 72809507-G-T

55631069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, missense_variant
orthologous variants: 72809483-C-T

55631070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 72809482-G-A

55631070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 72809482-G-T

55631189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72809359-T-G

http://identifiers.org/hco/15/GRCh38#55631197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72809351-A-C

55634373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72802856-C-T

55634496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72802741-G-T

55634516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72802721-T-G

http://identifiers.org/hco/15/GRCh38#55637021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72801436-C-A

55637021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72801436-C-T

http://identifiers.org/hco/15/GRCh38#55637023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72801434-C-A

55637023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72801434-C-T

55637046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72801411-A-T

55637104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72801347-T-C

55637104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72801347-T-G

http://identifiers.org/hco/15/GRCh38#55637153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72801291-C-A

55637153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72801291-C-T

55637375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72801068-G-C

55637375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72801068-G-T

55637625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72800668-T-C

55637681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72800538-A-G

http://identifiers.org/hco/15/GRCh38#55637853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72800373-C-A

55638321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72799764-C-T

55639554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72799349-G-C

55639554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72799349-G-T

http://identifiers.org/hco/15/GRCh38#55639555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72799348-C-A

55639555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72799348-C-G

55639555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72799348-C-T

55639588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72799315-G-A

55639588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72799315-G-T

55639678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72799239-C-T

55639693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72799224-C-T

55639717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72799200-G-A

55639922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72799000-G-A

55639922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72799000-G-C

55639938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72798984-T-C

http://identifiers.org/hco/15/GRCh38#55639939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72798983-C-A

http://identifiers.org/hco/15/GRCh38#55639969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72798955-A-C

55639969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72798955-A-G

55639969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72798955-A-T

55639971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72798953-G-C

55639971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72798953-G-T

http://identifiers.org/hco/15/GRCh38#55640044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72798882-C-A

55640044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72798882-C-T

55640531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72798470-T-C

55640536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72798465-G-A

55640546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72798460-A-G

55641056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72798199-G-C

55641097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72798167-C-T

55641115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 72798150-A-G

55641265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72797999-T-C

55641346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72797924-A-G

55641346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72797924-A-T

55642772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72797042-G-C

55645793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72795046-C-T

55645824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72795016-C-G

55645824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72795016-C-T

55646862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72793721-A-T

55646931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72793658-T-C

55646940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72793649-C-G

55646953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72793636-T-C

55647486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72792802-T-G

55647850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72792432-T-G

55647981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72792268-G-A

55648258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, undefined
orthologous variants: 72791939-C-T

55648365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, undefined
orthologous variants: 72791838-G-A

55648395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, undefined
orthologous variants: 72791814-G-A

55648395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, undefined
orthologous variants: 72791814-G-T

55649950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72790985-T-G

55650032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72790906-G-A

55650070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72790868-A-G

55650094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72790815-T-C

55650220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72790735-T-G

55650298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72790662-G-A

55650298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72790662-G-C

55650298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72790662-G-T

55650572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72790440-G-T

55651033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72790298-G-A

55651543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72788958-A-G

55652433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72787825-G-C

http://identifiers.org/hco/15/GRCh38#55652486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72787771-C-A

55652565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72787692-G-A

55652567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72787690-C-T

55653445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72786780-A-G

55653541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72786771-G-T

55653886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72786646-G-T

55654081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72786505-T-C

55654081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72786505-T-G

55654113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72786473-T-C

55654188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72786401-T-C

55654507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72785873-G-T

55655045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72785364-A-G

55655207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72785184-C-T

55658923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72782310-C-T

55658964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72782271-G-A

55659058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72782189-G-A

55659091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72782162-G-T

55659200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72782077-T-A

55659200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72782077-T-C

http://identifiers.org/hco/15/GRCh38#55659476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72781630-C-A

55659476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72781630-C-G

55659620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72781481-A-G

55659694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72781372-G-A

55659696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72781370-C-T

55660283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72780454-A-G

55660331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72780406-A-G

55660531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72780215-G-A

55660683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72780085-A-T

55660759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72780050-A-G

55660779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72780030-T-C

55661124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72779735-T-A

55661162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72779564-C-T

55661302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72779432-A-T

http://identifiers.org/hco/15/GRCh38#55661312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72779425-C-A

http://identifiers.org/hco/15/GRCh38#55661383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72779353-C-A

55661383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72779353-C-T

55661714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72779014-G-C

http://identifiers.org/hco/15/GRCh38#55661869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72778895-A-C

55661877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72778887-G-T

55661980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72778763-C-T

55662276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72778458-T-G

55662300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72778442-T-C

55662342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72778399-T-C

55668665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72772161-C-T

55668739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72772048-T-A

55668764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72771994-T-G

55668821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72771864-G-A

55668878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72771805-A-G

55669002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72771681-T-A

http://identifiers.org/hco/15/GRCh38#55669098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72771612-C-A

55669659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72771057-G-C

55669737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72770978-C-T

55669779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72770937-T-C

55669890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72770826-A-G

http://identifiers.org/hco/15/GRCh38#55669996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72770387-C-A

55670039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72769963-G-C

55670086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72769918-T-C

55671326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72768060-T-C

55671336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72768047-G-A

55671336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72768047-G-T

55672320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72766343-C-T

55672363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72766305-T-C

55672383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72766290-C-T

55672457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72766217-G-C

55672501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72766173-T-A

http://identifiers.org/hco/15/GRCh38#55672602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72766072-A-C

http://identifiers.org/hco/15/GRCh38#55672679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72765995-C-A

55672679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72765995-C-T

http://identifiers.org/hco/15/GRCh38#55672691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72765983-C-A

55672691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72765983-C-G

55672691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72765983-C-T

http://identifiers.org/hco/15/GRCh38#55673322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72764425-A-C

55673322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72764425-A-T

55673379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72764352-C-T

55673394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72764337-G-A

55673489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72764242-C-G

55673628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72764103-T-C

55673628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72764103-T-G

55673687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72764044-A-T

55673698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72764033-T-C

55673711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72764020-T-C

http://identifiers.org/hco/15/GRCh38#55673824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72763920-C-A

55673824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72763920-C-G

http://identifiers.org/hco/15/GRCh38#55673827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72763917-A-C

http://identifiers.org/hco/15/GRCh38#55673828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72763916-C-A

55673982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72763813-A-G

http://identifiers.org/hco/15/GRCh38#55673997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72763798-C-A

55675384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72762526-A-T

55675478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72762440-G-A

55675478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72762440-G-C

55675478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72762440-G-T

http://identifiers.org/hco/15/GRCh38#55675506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72762413-C-A

55675506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72762413-C-T

http://identifiers.org/hco/15/GRCh38#55675527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72762392-A-C

55675527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72762392-A-G

55675548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense_variant, undefined
orthologous variants: 72762371-T-A

http://identifiers.org/hco/15/GRCh38#55675569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72762350-A-C

55675671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72762248-T-C

http://identifiers.org/hco/15/GRCh38#55675790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72762003-C-A

55675790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72762003-C-T

55675802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72761991-G-A

55675802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72761991-G-T

55675809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72761984-T-C

55675816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72761983-T-C

55675817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72761982-G-A

55675817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72761982-G-T

55676099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72761724-T-C

55676295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72761537-A-G

55676295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72761537-A-T

55676448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72761393-A-G

55676740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72761102-A-T

55676900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72760950-C-G

55676953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72760901-C-T

http://identifiers.org/hco/15/GRCh38#55676954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72760900-C-A

55677723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72759071-G-A

55677723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72759071-G-T

55677754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72759047-T-C

55677756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72759045-G-C

55677756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72759045-G-T

55677760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72759041-G-A

55677760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72759041-G-T

55677761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72759040-G-T

55677768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72759033-T-C

55677958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72758847-C-T

55678092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72758708-T-C

http://identifiers.org/hco/15/GRCh38#55678153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72758661-A-C

55678153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72758661-A-G

http://identifiers.org/hco/15/GRCh38#55678165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72758649-C-A

55678165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72758649-C-G

55678581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72758108-A-T

55679033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72757413-T-C

55679121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72757344-T-C

55679192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72757283-A-T

55679473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72757007-T-C

55679502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72756977-G-A

55679502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72756977-G-C

55679502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72756977-G-T

http://identifiers.org/hco/15/GRCh38#55679542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72756938-C-A

http://identifiers.org/hco/15/GRCh38#55679731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72756358-C-A

55679731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72756358-C-T

55679770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72756329-T-C

55679788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72756313-G-C

55679789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72756312-A-G

55679858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72756259-A-G

55679917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72756203-T-C

55679917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72756203-T-G

55679986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72755817-A-G

55679986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72755817-A-T

55680017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72755785-G-A

55680017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72755785-G-C

55680017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72755785-G-T

55680020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72755782-A-G

55680089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72755717-T-A

55680089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense variant
orthologous variants: 72755717-T-C

55680230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72755576-C-T

http://identifiers.org/hco/15/GRCh38#55680252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72755557-A-C

55680252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72755557-A-G

http://identifiers.org/hco/15/GRCh38#55680316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72755504-A-C

55680404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72755418-G-T

55680451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72755371-T-C

55680482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72755336-A-G

55680482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72755336-A-T

http://identifiers.org/hco/15/GRCh38#55680538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72755279-C-A

55680538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72755279-C-T

55680589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72755228-G-A

55680589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72755228-G-T

55680700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72755136-T-C

55682253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72752399-A-T

55682290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72752356-T-C

55682299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72752343-G-A

55682299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72752343-G-T

55682410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: synonymous variant
orthologous variants: 72752225-T-C

55682511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72752123-A-G

http://identifiers.org/hco/15/GRCh38#55683044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72751823-A-C

55683105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72751758-G-C

55683166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72751688-C-T

55683253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72750537-A-G

55683352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72750471-T-C

55683459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72750443-C-G

55683485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72750429-G-C

55683647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72750279-T-C

55683648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72750278-A-T

55683664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72750262-A-T

http://identifiers.org/hco/15/GRCh38#55683683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#72750243-C-A

55683683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, undefined
orthologous variants: 72750243-C-T

http://identifiers.org/hco/15/GRCh38#55683767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72750144-A-C

55683767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72750144-A-G

http://identifiers.org/hco/15/GRCh38#55683956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72749952-C-A

55684019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72749892-T-A

55684019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72749892-T-C

http://identifiers.org/hco/15/GRCh38#55684046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72749872-C-A

55684046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72749872-C-T

http://identifiers.org/hco/15/GRCh38#55684214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72749701-A-C

55684536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72749415-G-C

http://identifiers.org/hco/15/GRCh38#55684561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72749372-A-C

55684561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72749372-A-G

55684620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72749336-A-T

55684898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72749067-T-C

55685172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72748816-G-T

55685202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72748804-T-C

55685303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72748614-G-A

55685412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72748413-T-C

http://identifiers.org/hco/15/GRCh38#55685604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72748215-C-A

55690092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72745865-A-G

55690155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72745803-T-C

55690164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72745794-C-G

55694693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72744414-T-C

55694707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72744402-T-G

55694710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72744399-A-G

55694837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72744277-C-T

55694844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72744270-T-C

55694952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72744171-T-C

55694952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72744171-T-G

55694975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72744148-C-G

55695199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72743932-A-G

55696389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72743131-T-C

55699566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72741589-T-A

55699593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72741558-T-A

55699681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72741478-G-C

55699802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72741390-C-T

http://identifiers.org/hco/15/GRCh38#55699826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72741370-A-C

55702312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72738074-G-A

http://identifiers.org/hco/15/GRCh38#55702465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72737986-C-A

http://identifiers.org/hco/15/GRCh38#55702538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72737814-A-C

55703526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72737422-G-C

55703555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72737393-A-G

55703561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72737387-A-T

http://identifiers.org/hco/15/GRCh38#55703688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72736601-C-A

55704134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72736151-C-G

55715152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72733448-A-G

55715723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72732931-T-G

http://identifiers.org/hco/15/GRCh38#55716365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72732289-C-A

55716472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72732184-G-A

55716569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72732087-G-A

55716569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72732087-G-C

55716818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72730247-C-G

55716825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72730237-T-C

55716835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72730227-A-G

55716842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72730220-T-C

55716844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72730218-T-C

55716859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72730203-A-G

55716873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72730189-C-T

55716889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72730136-A-G

http://identifiers.org/hco/15/GRCh38#55717150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72729426-A-C

55717464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72729098-T-A

http://identifiers.org/hco/15/GRCh38#55717510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72729052-A-C

55717514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72729048-T-C

http://identifiers.org/hco/15/GRCh38#55734504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72723543-C-A

55734635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72723420-C-T

55734720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72723327-T-A

55735163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72722935-G-A

55735163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72722935-G-T

http://identifiers.org/hco/15/GRCh38#55735164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72722934-A-C

55735165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72722933-T-C

55735220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72722654-C-G

55735296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72722579-T-C

55735512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72722038-G-C

55735512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72722038-G-T

55735522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72722026-C-G

55735522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72722026-C-T

55735594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72721948-A-G

55735653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72721885-A-G

http://identifiers.org/hco/15/GRCh38#55735683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72721811-A-C

55735683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72721811-A-T

55735687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72721808-T-A

55736051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72721484-A-G

55736129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72721406-A-G

55736417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72721161-A-T

55736470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72721112-C-T

55736478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72721104-T-C

55736521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72721079-T-G

55736550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72721049-T-C

55736578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72721022-C-T

55736611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72720990-T-C

http://identifiers.org/hco/15/GRCh38#55737047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72720570-A-C

55737419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, undefined
orthologous variants: 72720172-C-T

55737645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72719962-G-A

55737645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72719962-G-T

55737789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, undefined
orthologous variants: 72719758-G-C

55737849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, undefined
orthologous variants: 72719709-T-C

55737959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72719577-T-C

55737977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72719559-T-G

http://identifiers.org/hco/15/GRCh38#55738369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72718868-C-A

55738401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72718830-T-C

55738507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 72718724-A-G

55738549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72718666-T-C

55738899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72718490-G-A

55739014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72718443-T-G

55739247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72718201-A-G

55740988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72716478-G-A

55741116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72716347-T-C

55741329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72716130-G-T

55741353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72716106-G-A

55741632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72715874-G-A

55741632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72715874-G-C

55741649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72715857-G-A

55741748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72715734-A-T

http://identifiers.org/hco/15/GRCh38#55741907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72715587-C-A

55742117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72715314-G-A

55742117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72715314-G-T

55742122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72715309-G-A

55742131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72715300-T-C

http://identifiers.org/hco/15/GRCh38#55742294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#72715187-C-A

55742294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 72715187-C-T

55742311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 72715170-T-C

55742486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 72715004-G-A

55742486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 72715004-G-C

55742486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 72715004-G-T

55742531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 72714975-G-A

55742531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 72714975-G-T

55742714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26373
most severe consequence: intron variant
orthologous variants: 72714893-T-C