55250826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3569455-A-G

55250839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3569442-T-A

55250967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3569322-G-A

55251465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3569016-T-C

55251491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3568989-C-T

55251499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3568979-G-A

55251592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3568886-A-G

55251608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3568870-A-T

http://identifiers.org/hco/8/GRCh38#55251916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3568567-C-A

http://identifiers.org/hco/8/GRCh38#55252109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3568377-C-A

55252109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3568377-C-T

55252159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3568330-A-G

55252285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3568215-G-A

55252662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3567914-A-G

55253226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3567354-A-G

55253344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3567243-C-G

55253344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3567243-C-T

55253358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3567229-C-T

55253478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3567121-A-G

55253637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3566956-G-C

55254137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3566768-A-G

55254201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3566700-G-A

55254981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3565919-A-T

55255242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3565673-C-T

55255246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3565669-C-T

http://identifiers.org/hco/8/GRCh38#55255319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3565593-C-A

55255566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3565191-T-A

55255568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3565189-A-G

55255704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3565052-A-G

55259215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3563706-C-T

55259263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3563659-C-T

55259573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3563370-C-T

55259576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3563367-C-T

55259669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3563296-C-G

55259779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3563186-C-T

http://identifiers.org/hco/8/GRCh38#55260304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3562733-A-C

55260335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3562702-T-C

55261860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3560129-G-A

http://identifiers.org/hco/8/GRCh38#55261933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3560031-C-A

55261933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3560031-C-T

55263016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3557245-C-T

55263258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3557010-C-G

55263276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3556992-T-C

55263299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3556972-C-T

55263337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3556932-C-G

55263468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3556789-A-T

55263614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3556477-A-G

55263764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3556316-C-T

55263779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3556302-G-A

55263935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3556137-G-A

55264049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3556054-G-A

55264056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3556047-A-T

http://identifiers.org/hco/8/GRCh38#55264178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3555931-C-A

55264311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3555816-G-C

http://identifiers.org/hco/8/GRCh38#55264346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3555783-C-A

55264767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3555399-A-G

55264896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3555259-A-G

55265204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3554892-A-T

55265235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3554860-C-T

55266253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3554671-C-T

55266255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3554669-C-G

http://identifiers.org/hco/8/GRCh38#55266289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3554653-C-A

55266289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3554653-C-T

55266686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3554309-T-A

55270697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3551935-A-G

55272033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3548851-G-T

55272293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3548328-G-A

55272453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3548183-A-G

55272476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3548151-T-C

55272532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3548120-C-T

http://identifiers.org/hco/8/GRCh38#55272870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3547855-C-A

http://identifiers.org/hco/8/GRCh38#55273008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3547719-C-A

55273008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3547719-C-T

55273028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3547699-G-A

http://identifiers.org/hco/8/GRCh38#55273037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3547690-C-A

55273178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3547516-G-A

55274897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3546044-T-C

55275272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3545231-A-G

55275451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3545068-T-C

55275900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3544637-C-T

55276901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3541740-A-T

55276948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3541702-T-A

55276963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3541687-T-C

55277011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3541637-C-T

55277030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3541618-A-T

http://identifiers.org/hco/8/GRCh38#55277131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3541546-C-A

55277181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3541499-T-G

55277266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3541424-T-C

55277687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3541087-C-T

55278001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3540831-T-G

55283789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3540517-G-T

55283866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3540439-T-C

55283883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3540422-G-A

55283918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3540389-T-G

55284209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3540167-T-A

55284288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3540095-T-C

55284366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3540018-T-C

55284448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3539935-G-A

55284584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3539815-A-G

55286164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3538169-C-T

55286166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3538167-A-G

55286263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3538069-G-A

55287244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3537377-C-T

http://identifiers.org/hco/8/GRCh38#55287303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3537318-A-C

55287469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3537179-G-A

55287469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3537179-G-T

55287666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3537022-C-T

55288259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3536735-G-T

55288638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3536360-T-C

55288740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3536271-A-G

55288751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3536260-T-C

55288751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3536260-T-G

55288822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3536191-C-T

55295081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3532741-A-G

55295185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3532647-A-T

55295200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3532632-C-T

55295291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3532541-G-A

55295291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3532541-G-C

55295325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3532528-A-G

55295654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3532263-A-T

55295660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3532257-C-T

55295861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3532059-G-A

55296104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3531826-T-C

55296384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3531569-T-C

55296557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3531431-T-A

55296557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3531431-T-C

55296590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3531401-C-T

55296639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3531366-A-G

55296990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3529201-G-C

55297149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3529069-A-G

55297250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3528975-G-A

55297250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3528975-G-C

55297250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3528975-G-T

55297563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3528659-C-T

55297691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3528538-A-G

http://identifiers.org/hco/8/GRCh38#55299174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3527217-C-A

55299174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3527217-C-T

55299710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3526638-C-T

55300105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3525964-C-T

55300328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3525719-G-A

55300388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3525659-C-T

55300953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3524932-G-T

55305009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3524799-A-G

55305009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3524799-A-T

55305033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3524780-A-G

55305535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3524157-A-G

55305644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3524056-T-G

55305809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3523895-T-C

55306087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3523629-A-G

55306103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3523613-G-T

http://identifiers.org/hco/8/GRCh38#55306180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3523533-A-C

55311070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3522048-C-G

55311162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3521962-G-A

55311256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3521875-A-G

55311297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3521835-A-G

55311695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3521473-T-C

55311703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3521465-A-G

55311746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3521422-T-C

55311813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3521357-T-C

55311813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3521357-T-G

55311814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3521356-G-C

55311814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3521356-G-T

http://identifiers.org/hco/8/GRCh38#55311816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3521354-C-A

55311816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3521354-C-T

http://identifiers.org/hco/8/GRCh38#55311875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3521322-C-A

55312184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3521012-C-T

55312198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3520987-A-T

http://identifiers.org/hco/8/GRCh38#55312425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3520743-C-A

55312433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3520732-G-C

55312542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3520632-A-G

55312657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3520520-T-A

55312657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3520520-T-C

55312704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3520475-T-C

http://identifiers.org/hco/8/GRCh38#55313340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3518767-C-A

55313340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3518767-C-T

55313416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3518690-G-C

55313884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3518104-C-G

55313884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3518104-C-T

55314469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3517541-C-G

55314469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3517541-C-T

55314477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3517533-C-G

55314621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3517396-G-A

55316771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3515270-A-G

55316783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3515258-A-T

55316960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3515082-A-G

55318459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3512545-T-G

http://identifiers.org/hco/8/GRCh38#55318618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3512369-A-C

55318690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3512289-T-C

55318764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3512212-C-T

55318863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3512116-G-C

55320210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3510494-G-A

55321041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3509055-T-A

55321152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3508938-C-T

55321220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3508875-A-G

55326803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3507116-G-A

55326923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3506996-A-G

55326967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3506951-T-A

55327084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3506762-T-A

55327225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3506595-A-G

55327319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3506501-A-G

55327372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3506424-T-C

http://identifiers.org/hco/8/GRCh38#55327476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3506321-C-A

55327667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3506123-A-G

55327834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3505952-T-C

55327943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3505852-G-A

55337287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3505272-T-C

55337316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3505247-T-C

55337452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3505155-A-G

55337582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3505035-G-T

55337786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3504855-T-G

55337836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3504806-A-G

55337883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3504730-T-C

55337891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3504722-G-A

55337974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3504639-C-G

55337982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3504631-T-C

55338183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3504428-T-C

55338449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3504182-C-T

55338572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3504082-T-C

55338611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3504044-C-T

55338846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3503903-C-T

55338966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3503801-G-A

55338966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3503801-G-T

55339084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3503684-T-A

55339099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3503669-A-G

55339977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3502873-T-C

55340076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3502780-T-C

55340124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3502730-T-G

55340151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3502704-A-T

55340311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3502548-C-T

55340437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3502424-A-G

55340472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3502394-G-C

55340884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3501839-G-A

55341129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3501610-G-T

55341158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3501576-T-C

55342679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3500358-G-A

55342908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3500142-A-G

55343185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3499887-G-A

55343198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3499874-A-G

55343424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3499718-A-G

55343950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3499201-G-A

55343980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3499175-G-C

55343993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3499162-T-C

55344322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3498856-C-T

55346732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3498498-A-G

55346769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3498461-G-A

http://identifiers.org/hco/8/GRCh38#55346899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3498333-A-C

55347768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3497985-T-A

55347807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3497950-A-G

55351189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3496542-T-A

55351551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3496203-T-C

55351714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3496088-T-C

55352299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3495575-G-A

55352317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3495556-G-A

55357270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3492514-C-T

55357320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3492462-C-T

55357518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3492267-T-C

55357529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3492254-T-G

55357576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3492212-G-T

55357588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3492200-A-G

55357589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3492199-T-C

55357922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3491882-T-C

55358660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3491472-A-G

55358795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3491341-G-C

55358816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3491317-C-T

55358915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3491224-G-A

55358917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3491222-G-A

55358988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3490522-G-T

55359185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3489391-G-T

55359352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3489133-G-A

55359352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3489133-G-T

55359393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3489093-A-G

55359459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3489038-T-A

55359609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3488852-C-T

55359623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3488833-A-G

55359765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3488607-C-T

55359815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3488547-G-A

55360301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3488081-G-C

55360345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3488057-C-G

55360407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3487998-T-G

55360741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3487662-T-G

55361056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3487196-A-G

55361158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3487106-G-A

55361967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3486510-C-T

55362125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3486351-G-T

55362149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3486327-C-T

55362317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3486176-G-A

55362351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3486142-C-T

55363169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3484747-C-G

55363182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3484734-C-T

55363406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3483982-C-T

55363531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3483857-C-T

55363677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3483732-C-T

55363782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3483626-G-A

55363795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3483613-C-G

55363842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3483566-T-A

55364498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3482454-C-T

55364525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3482427-A-G

55365016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3482314-G-A

55365141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3482216-G-C

55365184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3482169-G-C

55365240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3482120-G-A

55365975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3481308-C-G

55366060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3481236-C-G

55366126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3481169-A-G

http://identifiers.org/hco/8/GRCh38#55366200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3481102-C-A

55366610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3480768-T-G

http://identifiers.org/hco/8/GRCh38#55366673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3480691-A-C

55366697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3480666-A-G

55366928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3480346-T-A

55366928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3480346-T-C

55367060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3480166-C-T

55367186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3480048-A-T

55367432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3479793-A-G

http://identifiers.org/hco/8/GRCh38#55367455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3479774-C-A

55367455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3479774-C-T

55367540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3479685-T-C

55367665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3479555-A-T

55367859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3479383-C-T

55368518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3479066-C-T

55368705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3478881-T-C

55371109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3478584-T-A

55371109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3478584-T-C

55371314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3478352-G-A

55372014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3477612-T-C

55372591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3477040-C-T

55372823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3476831-G-A

http://identifiers.org/hco/8/GRCh38#55372864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3476784-C-A

55372864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3476784-C-T

55372887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3476761-T-C

55372908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3476733-T-C

55372924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3476717-G-A

55373599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3475965-C-T

55373835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3475714-G-T

55373992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3475568-C-T

55374275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3475323-G-A

55377011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3471033-T-A

http://identifiers.org/hco/8/GRCh38#55378196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3469985-A-C

55378276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3469907-A-G

55378486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3469696-G-A

55378486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3469696-G-C

55378486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3469696-G-T

55378597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3469585-T-C

55378778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3469395-A-G

http://identifiers.org/hco/8/GRCh38#55378779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3469394-A-C

55378900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3469273-A-G

http://identifiers.org/hco/8/GRCh38#55379044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3469125-A-C

55379470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3467984-G-A

55379984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3467583-C-T

55380159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3467414-G-A

55380348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3467223-C-G

http://identifiers.org/hco/8/GRCh38#55380677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3466913-A-C

55380947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3466706-A-T

55381186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3466558-T-C

55381186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3466558-T-G

55381187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3466557-T-C

55381223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3466521-T-G

55382024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3466118-T-C

55382409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3465730-T-G

55382539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3465598-G-A

55383387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3464223-G-A

55383433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3464179-G-A

55383461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3464151-T-C

55383463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3464149-C-T

55383492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3464134-G-C

55383690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3463950-T-A

55383752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3463887-G-A

55383818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3463838-G-A

55383853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3463803-G-C

55384084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3463633-A-G

55384325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3463468-G-A

55384553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3463053-G-A

55384834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3462775-T-C

55388367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3460106-T-A

55388380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3460093-G-T

55388470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3460012-G-C

http://identifiers.org/hco/8/GRCh38#55388532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3459964-A-C

55388532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3459964-A-G

55389098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3459463-C-T

http://identifiers.org/hco/8/GRCh38#55389320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3459264-C-A

55389320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3459264-C-G

55389518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3459072-T-C

http://identifiers.org/hco/8/GRCh38#55389570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3459018-A-C

55389700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3458887-T-C

55389876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3458714-C-T

55390172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3458434-A-G

55390246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3458364-C-T

55393231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3457326-G-C

55393332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3457244-G-A

55393332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3457244-G-T

http://identifiers.org/hco/8/GRCh38#55393549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3457053-C-A

55393549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3457053-C-G

55393549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3457053-C-T

55393600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3456992-T-C

55393676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3456916-T-C

55393831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3456774-T-A

55393834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3456771-T-A

55393834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3456771-T-C

55393980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3456630-A-G

55394072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3456531-T-C

55394111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3456492-T-C

55394127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3456477-A-G

55394456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3456159-C-T

http://identifiers.org/hco/8/GRCh38#55394457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3456158-A-C

55394645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3456014-A-G

55394746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3455915-T-C

55395246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3455171-G-A

55395279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3455148-G-A

55395376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3455052-G-A

55395379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3455049-T-A

55395383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3455045-G-C

55395827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3453565-G-A

http://identifiers.org/hco/8/GRCh38#55395829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3453563-C-A

55395829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3453563-C-T

55395942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3453475-C-G

55396029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3453414-T-G

55396085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3453370-C-T

55396217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3453249-A-G

55396313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3453167-A-G

55396418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3453104-T-G

55398323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3452833-C-T

55398424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3452728-T-C

55398438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3452708-A-G

http://identifiers.org/hco/8/GRCh38#55398616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3452541-C-A

55398648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3452509-A-G

55398764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3452397-A-G

http://identifiers.org/hco/8/GRCh38#55398787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3452375-A-C

55398825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3452341-C-T

55398886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3452291-A-G

55399352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3451847-A-G

http://identifiers.org/hco/8/GRCh38#55400378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3450614-C-A

http://identifiers.org/hco/8/GRCh38#55400746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3450015-C-A

55400879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3449880-A-G

http://identifiers.org/hco/8/GRCh38#55400896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3449870-C-A

55401207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3449354-T-A

55401476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3449100-T-G

55401508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3449064-G-T

55401823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3448764-T-C

http://identifiers.org/hco/8/GRCh38#55402780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3443113-A-C

55404168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3442763-T-C

55404233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3442695-T-A

55404233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3442695-T-C

55404250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3442675-T-A

http://identifiers.org/hco/8/GRCh38#55404304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3442584-C-A

55404312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3442553-A-T

http://identifiers.org/hco/8/GRCh38#55404708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3442140-A-C

55404858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3442012-G-A

55404858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3442012-G-C

http://identifiers.org/hco/8/GRCh38#55404989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3441880-C-A

55405203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3441669-A-G

55409139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3439732-G-A

55409361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3439538-G-C

55409702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3439202-T-C

55409949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3438697-C-T

55410194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3438451-T-C

55410288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3438379-T-C

55410421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3438262-A-G

55410549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3438131-A-G

55411567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3437678-A-G

55411700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3437549-C-T

55411750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3437501-T-G

55411993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3437264-A-T

55412110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3437154-C-T

55412290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3436980-G-A

55412434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3436807-C-T

55412498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3436735-C-G

55412498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3436735-C-T

55412598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3436641-T-C

55412687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3436553-A-G

http://identifiers.org/hco/8/GRCh38#55412691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3436549-A-C

55412925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3436355-T-A

55413945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3435630-T-C

55414618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3434342-A-G

55414655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3434307-C-G

55414706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3434258-A-G

55414833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3434128-C-T

55414930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3434052-A-G

http://identifiers.org/hco/8/GRCh38#55415173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3433861-A-C

55415440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3433616-A-T

55415538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3433526-A-G

55416004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3432601-A-G

55416032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3432574-T-C

55416110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3432495-G-C

55416305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3432311-A-G

55417193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3431467-T-C

55417236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3431423-C-G

55417236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3431423-C-T

55417366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3431302-A-T

55417383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3431283-T-G

55417900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3430805-G-A

55418057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3430684-C-T

55418356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3430442-A-G

55418410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3430394-T-G

55418782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3430003-C-T

55418821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3429962-A-T

55418837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3429953-C-T

55419312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3429703-G-A

55419944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3429156-A-G

55420827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3428861-A-T

http://identifiers.org/hco/8/GRCh38#55421252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3428416-C-A

55421326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3428343-T-A

55421362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3428307-C-T

55422342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3428256-A-G

55422737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3427877-T-C

55423597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3427145-G-T

55423866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3426920-A-G

55423902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3426884-G-A

55423925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3426857-T-C

55424019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3426766-A-G

55424164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3426593-G-T

55424591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3426183-T-A

http://identifiers.org/hco/8/GRCh38#55424634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3426140-C-A

55427069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3424523-G-A

55427365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3424240-A-G

55427681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3424078-T-G

55428047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3423623-A-G

55428179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3423466-A-G

55428558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3423113-G-C

55428595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3423070-G-T

55428628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3423037-C-T

55428775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3422913-A-G

55429000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3422709-G-C

55430192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3404621-T-C

55430272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3404543-C-T

55430336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3404481-A-G

55430386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3404430-T-A

55430386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3404430-T-G

55430508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3404221-T-C

55430508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3404221-T-G

55430842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3403865-G-A

55430887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3403816-G-C

55432767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3397102-A-G

55432843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3397035-G-A

55432911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3396968-T-G

http://identifiers.org/hco/8/GRCh38#55433002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3396915-C-A

55433021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3396894-G-A

55433239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3396684-G-T

http://identifiers.org/hco/8/GRCh38#55433352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3396587-C-A

55433428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3396528-C-T

55433455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3396503-T-G

55433461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3396497-C-G

55433464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3396494-A-G

55433625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3396338-C-T

55433737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3396240-G-T

55434272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3395124-T-C

55434414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3394982-T-G

55434598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3394816-T-G

55434719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3394697-G-A

55434754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3394675-C-T

55434804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3394606-C-T

55436270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3392979-C-G

55436337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3392908-A-G

55436957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3392292-A-T

http://identifiers.org/hco/8/GRCh38#55436981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3392268-A-C

55437085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3392160-G-A

55438101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3391271-G-A

55438133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3391239-G-A

55438154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3391220-A-G

55438638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3391033-G-A

55438760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3390915-A-G

55446718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3381444-G-T

55446857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3381367-T-C

55446913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3381305-A-G

55446917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3381301-T-C

55447499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3380914-G-A

http://identifiers.org/hco/8/GRCh38#55447562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3380856-A-C

55447674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3380750-C-G

http://identifiers.org/hco/8/GRCh38#55447889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3380536-C-A

55447914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3380511-T-C

55447914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3380511-T-G

55448895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3379569-A-T

55468034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3367980-C-T

55468160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3367869-C-T

55468215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3367814-G-A

55468321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3367720-T-C

55468401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3367647-G-A

55468401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3367647-G-T

55468727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3367364-T-A

55469395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3366863-A-T

55469420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3366844-T-C

55470236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3365368-T-A

55470668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3365298-A-G

55471000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3365024-T-C

55472287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3364238-G-T

55472510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3364021-A-G

55472656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3363882-G-A

55472656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3363882-G-T

55472746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3363791-A-G

55472947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3363611-G-A

55473308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3363274-T-A

55473308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3363274-T-C

55473369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3363212-T-A

55473709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3362897-T-C

55474249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3362808-C-T

55474530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3360941-T-C

55474569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3360907-C-T

55474719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3360761-A-G

55474901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3360565-G-C

55474933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3360532-T-C

55475145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3360350-A-G

55475163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3360332-A-G

55482717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3359914-T-A

55483283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3359336-T-G

55483304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3359315-G-T

55483435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3359185-G-A

55483452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3359168-C-T

http://identifiers.org/hco/8/GRCh38#55483537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3359085-C-A

55483537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3359085-C-T

http://identifiers.org/hco/8/GRCh38#55483557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3359064-C-A

55497410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3337430-G-A

55497423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3337407-T-C

55497744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3337133-C-T

55497809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3337067-T-C

55499292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3335565-T-C

55499651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3335220-T-C

55499737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3335147-C-T

55507184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3325624-C-T

55508108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3325417-A-G

55508177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3325348-A-T

55508180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3325345-T-C

http://identifiers.org/hco/8/GRCh38#55508316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3325208-C-A

55508316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3325208-C-T

55508594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3324922-G-T

55509686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3320432-C-T

55509895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3320232-T-C

55509989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3320164-C-T

55510199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3319993-G-A

55510206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3319986-C-T

55511184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3319295-C-G

55512581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3297946-T-C

55512691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3297836-T-C

55512740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3297783-T-C

55512740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3297783-T-G

55513379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3297214-A-G

55513565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3297020-T-C

55515065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3296443-T-C

55515272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3296244-C-T

55515329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3296178-A-T

55515347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3296160-T-A

55515588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3295954-A-G

55515588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3295954-A-T

55518199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3294219-C-G

55518320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3294105-A-G

55518417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3294027-T-A

55518442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3294002-C-T

55518476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3293962-C-T

55518711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3291228-A-G

55518764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3291191-G-T

55518951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3291033-T-C

55519159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3290877-T-C

55519253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3290787-T-C

http://identifiers.org/hco/8/GRCh38#55519475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3290577-C-A

http://identifiers.org/hco/8/GRCh38#55519609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3290454-C-A

55519609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3290454-C-G

55520114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3290201-C-T

55520173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3290142-T-C

55521534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3288618-A-G

55521622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3288533-G-T

55521635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3288522-G-T

http://identifiers.org/hco/8/GRCh38#55522036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3288158-C-A

55522172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3288048-G-A

http://identifiers.org/hco/8/GRCh38#55522252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3287985-A-C

55522473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3287774-T-C

55522599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3287647-A-G

55522850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3287405-A-G

http://identifiers.org/hco/8/GRCh38#55523207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3287266-C-A

55523207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3287266-C-T

55523212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3287261-C-G

55523212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: intron variant
orthologous variants: 3287261-C-T

http://identifiers.org/hco/8/GRCh38#55523505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3286965-A-C

55523811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: missense variant
orthologous variants: 3286659-T-C

55523865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: missense variant
orthologous variants: 3286605-C-G

55523865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: missense variant
orthologous variants: 3286605-C-T

55524228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3286242-A-G

http://identifiers.org/hco/8/GRCh38#55524248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3286231-C-A

55524337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3286143-G-C

55524337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3286143-G-T

55524423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3286064-G-T

http://identifiers.org/hco/8/GRCh38#55524488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3286018-C-A

55524488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3286018-C-T

55524764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3285591-C-T

55525107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3285261-C-G

55525107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3285261-C-T

55525178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3285168-G-A

55525178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3285168-G-T

55525182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3285164-A-G

55525195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3285158-G-T

55525199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3285154-G-C

55525229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3285130-T-C

http://identifiers.org/hco/8/GRCh38#55525230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3285129-C-A

55525230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3285129-C-G

http://identifiers.org/hco/8/GRCh38#55525618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3284756-C-A

55526068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3284310-G-T

55526353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 3284045-A-G

http://identifiers.org/hco/8/GRCh38#55526468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3283931-C-A

55526609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 3283790-G-T

55526660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 3283739-A-G

55526710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 3283694-A-G

55526848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3283577-C-G

55526853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3283575-A-G

55526853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3283575-A-T

55526857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3283571-G-T

55526966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3283466-G-A

55527605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3282894-G-T

55527664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3282831-A-T

55527723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3282772-C-T

55528147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3281663-T-C

55528540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3281312-G-A

55528540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3281312-G-T

http://identifiers.org/hco/8/GRCh38#55528547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3281305-C-A

55528578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3281274-T-A

55528578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3281274-T-C

55528863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3280961-G-A

55528863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3280961-G-T

55528915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3280909-C-G

55528915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3280909-C-T

55528916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3280908-G-A

55528916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3280908-G-T

55528940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3280885-G-A

55528940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3280885-G-T

55529218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3280602-G-A

55529218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3280602-G-T

55529550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3280147-C-G

55529564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3280135-T-C

http://identifiers.org/hco/8/GRCh38#55530066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3279604-C-A

55530077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3279593-A-T

http://identifiers.org/hco/8/GRCh38#55530465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3279380-C-A

http://identifiers.org/hco/8/GRCh38#55530886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3278999-C-A

http://identifiers.org/hco/8/GRCh38#55531028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3278871-C-A

55531028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3278871-C-T

55532314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3278614-T-C

55532433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3278521-G-A

http://identifiers.org/hco/8/GRCh38#55532490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3278466-C-A

55532919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3278353-A-G

55532951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3278320-A-G

55533481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3277687-G-A

55533584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3277607-A-G

55533632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3277561-G-A

55533812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 3277383-G-A

55533812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 3277383-G-T

55534741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3276789-T-C

55534770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3276779-T-G

http://identifiers.org/hco/8/GRCh38#55534852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3276714-A-C

55534994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3276586-A-G

55535102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3276506-T-C

http://identifiers.org/hco/8/GRCh38#55535113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3276495-A-C

55535127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3276481-G-A

55535127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3276481-G-C

55535205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3276405-G-A

55535554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3276304-G-A

55535630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3276230-G-T

55535689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3276186-G-T

http://identifiers.org/hco/8/GRCh38#55535748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3276128-C-A

55535793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3276083-G-A

55535793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3276083-G-T

55535907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3275970-G-A

55535907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3275970-G-C

55536145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3275763-T-C

55536257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3275655-A-G

http://identifiers.org/hco/8/GRCh38#55536300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3275611-C-A

55536405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3275507-T-A

55536541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3275368-A-T

http://identifiers.org/hco/8/GRCh38#55536664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3275250-C-A

55536826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3275060-G-A

55536921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3274967-T-C

55537217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3274679-C-T

http://identifiers.org/hco/8/GRCh38#55537273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3274624-C-A

55537318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3274589-T-C

55537376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3274539-T-A

55537376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3274539-T-C

55537384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3274535-G-T

55537402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3274511-C-G

55537756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3274171-T-A

55537760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3274167-G-A

55538128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3273800-T-C

55538211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3273718-C-T

55538299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3273630-A-G

55538356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3273577-G-A

55538356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3273577-G-T

55538406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3273527-G-A

55538406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3273527-G-T

55538414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3273519-A-G

55538452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3273489-G-T

55538687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3273285-T-C

http://identifiers.org/hco/8/GRCh38#55538726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3273256-C-A

55538735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3273247-A-G

55538856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3273143-A-G

55538902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3273102-A-G

55539410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3272641-G-A

55539449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3272602-T-C

http://identifiers.org/hco/8/GRCh38#55539690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3272366-C-A

55539690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3272366-C-T

55539749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3272311-G-T

55539981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3272111-A-G

55539981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3272111-A-T

55540011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3272082-G-A

55540011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3272082-G-T

55540190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3271896-T-A

55540192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3271894-A-G

55540227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3271859-T-C

55540484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3271635-G-T

55540875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3271200-T-C

55540962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3271119-T-C

55540973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3271108-A-G

55541043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3271043-G-C

http://identifiers.org/hco/8/GRCh38#55541416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3270670-C-A

55541456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3270628-A-G

http://identifiers.org/hco/8/GRCh38#55541615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#3270489-C-A

55541661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29394
most severe consequence: 3 prime UTR variant
orthologous variants: 3270446-T-C