52075252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3 prime UTR variant
orthologous variants: 106227736-G-T

52075257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3 prime UTR variant
orthologous variants: 106227731-A-G

http://identifiers.org/hco/3/GRCh38#52075264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106227724-C-A

52075268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3 prime UTR variant
orthologous variants: 106227720-T-G

52075327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3 prime UTR variant
orthologous variants: 106227660-G-A

52075349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3 prime UTR variant
orthologous variants: 106227637-A-G

http://identifiers.org/hco/3/GRCh38#52075455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106227519-C-A

52075455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3 prime UTR variant
orthologous variants: 106227519-C-T

52075695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3 prime UTR variant
orthologous variants: 106227172-A-G

52075900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: missense variant
orthologous variants: 106226964-C-T

52075906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: missense variant
orthologous variants: 106226958-A-G

52075966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: missense variant
orthologous variants: 106226898-T-C

http://identifiers.org/hco/3/GRCh38#52076106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106226771-C-A

52076106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106226771-C-T

52076244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106226694-G-A

52076262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106226676-C-T

52076534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106226510-G-A

52077295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106226054-T-C

http://identifiers.org/hco/3/GRCh38#52077374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106225983-A-C

52077651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106225698-C-T

52077794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106225543-C-T

52077954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106225372-T-C

52078182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106225056-C-T

http://identifiers.org/hco/3/GRCh38#52078335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106224945-A-C

52078350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106224931-G-A

52078350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106224931-G-C

52078839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106224492-C-T

52078965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106224397-G-A

52078965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106224397-G-C

52079211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106224189-G-A

52079315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106224096-T-C

52079483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106223737-G-C

52082191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106222737-G-A

52082709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106222282-C-G

52082720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106222271-A-G

52082778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106222214-C-T

52082998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106222047-T-C

52083092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106221958-G-A

52083204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106221871-G-A

52083324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106221771-G-T

http://identifiers.org/hco/3/GRCh38#52083358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106221740-A-C

52083630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106221371-A-T

52083656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106221295-G-A

52083656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106221295-G-C

52083714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106221239-T-C

http://identifiers.org/hco/3/GRCh38#52084011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106220797-C-A

52084037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106220782-T-C

52084249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106220651-C-G

52084457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106220588-C-G

52084657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106220337-T-A

52084665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106220329-C-T

52084786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106220227-C-T

52085018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106220041-T-C

52085308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219873-G-A

http://identifiers.org/hco/3/GRCh38#52085325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106219857-C-A

http://identifiers.org/hco/3/GRCh38#52085402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106219795-C-A

52085417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219776-C-G

52085463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219742-T-C

52085463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219742-T-G

52085558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219680-T-A

52085558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219680-T-C

52085577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219659-G-A

52085621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219600-G-C

52085682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219542-C-T

52085725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219499-G-C

52085737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219490-G-A

52085758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219469-T-C

52086101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, undefined
orthologous variants: 106219149-C-T

52086106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219144-C-G

52086106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219144-C-T

52086239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106219007-C-T

52087649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106217662-A-G

52087875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106217343-C-T

52087929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106217296-A-G

http://identifiers.org/hco/3/GRCh38#52088158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106217161-A-C

52088166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106217153-C-T

52088189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106217130-C-T

52088202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106217117-C-T

52088504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106216668-A-G

52088716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, undefined
orthologous variants: 106216463-C-T

52088933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106216306-A-T

52088940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106216299-A-G

52089152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106216095-C-T

52089630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106215608-A-G

52089684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106215588-G-A

52090451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106214873-A-G

52090558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, undefined
orthologous variants: 106214784-G-A

52090596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106214749-G-A

52090963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106214455-G-A

52091116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106214215-G-A

52091409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106213845-C-T

http://identifiers.org/hco/3/GRCh38#52091762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106213467-C-A

52091810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106213423-A-T

52091926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106213208-C-T

52091978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106213145-G-A

52092045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106213111-G-C

52092448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106212220-T-C

http://identifiers.org/hco/3/GRCh38#52092804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106211697-C-A

52092880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106211620-G-A

52093211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106211328-G-T

52093274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106211269-G-A

52093316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106211231-C-G

52093978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106210317-G-A

52095026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106209598-T-C

52095159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106209481-G-C

52095407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106209292-G-A

52095434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106209265-G-A

52095535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106209189-C-T

52095632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106209112-G-A

52096044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106208752-C-T

52096078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106208718-C-T

http://identifiers.org/hco/3/GRCh38#52096111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106208689-C-A

http://identifiers.org/hco/3/GRCh38#52096426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106208409-A-C

52096426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106208409-A-G

52096426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106208409-A-T

52096473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106207295-T-C

http://identifiers.org/hco/3/GRCh38#52096554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106207225-C-A

52096554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106207225-C-T

52096555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron variant
orthologous variants: 106207224-A-G

52096570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 106207212-T-C

52096770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106207017-A-G

52096862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106206931-G-A

52096862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106206931-G-T

52096937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106206851-T-C

52096938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106206850-T-C

52097256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106206596-G-A

52097405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106206450-G-A

52097764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106205435-G-A

52098167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106205105-A-G

52098265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106205014-G-A

52098336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106204941-T-C

52098795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106204004-A-G

http://identifiers.org/hco/3/GRCh38#52099115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106203704-C-A

52099192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106203638-C-T

52099219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106203611-T-C

52099928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106202984-A-G

52099948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106202964-A-G

52104468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106200795-T-C

52104658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106200606-G-A

52104658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106200606-G-C

52104830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106200447-G-C

52105492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106199855-G-A

52105493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106199854-G-A

52105551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106199801-C-G

52105551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106199801-C-T

52105894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106199518-G-C

52105894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106199518-G-T

52106643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106199252-T-C

52106695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106199208-C-G

http://identifiers.org/hco/3/GRCh38#52106808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106199126-C-A

52107303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106198730-G-A

52107303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106198730-G-C

52107303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106198730-G-T

52107318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106198716-G-A

52107896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106197415-A-T

52108034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106197227-A-G

52108264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106197035-G-A

52108468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106196821-A-G

52108553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106196735-G-A

52108789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106196538-C-T

http://identifiers.org/hco/3/GRCh38#52109944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106195280-C-A

52110033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106195193-G-A

52110297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106194895-C-T

52110506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106194204-A-G

52110614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106194111-G-A

52111036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106193748-T-C

http://identifiers.org/hco/3/GRCh38#52112073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106193479-C-A

52112806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106193310-G-A

52113079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106193068-T-A

52115788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106191486-A-G

52115832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106191430-A-T

52115841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106191421-A-G

52116402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106191069-G-A

52116470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106191003-T-C

52117409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106190391-G-A

52117665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106190189-G-A

52117707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106190143-C-T

52117874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106189667-T-C

52117917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106189621-A-G

52119058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106188554-A-G

52119128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106188501-A-G

http://identifiers.org/hco/3/GRCh38#52119272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106188420-A-C

52119290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106188410-T-C

52119313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106188387-G-A

52119313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106188387-G-T

52119329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106188372-T-C

52120204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106187906-T-C

52120205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106187905-G-A

52120241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106187864-A-T

52120258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106187810-T-C

52120326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106187718-C-T

52120619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106187446-T-C

52120836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106187202-C-T

52120901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106187140-A-G

52120981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106186482-G-A

52121282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106186236-A-G

http://identifiers.org/hco/3/GRCh38#52121900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106185675-A-C

52121900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106185675-A-G

52122148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106185444-G-A

http://identifiers.org/hco/3/GRCh38#52122329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106185277-C-A

52122340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106185269-G-A

http://identifiers.org/hco/3/GRCh38#52122544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106185104-A-C

http://identifiers.org/hco/3/GRCh38#52122620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106185042-C-A

52122620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106185042-C-G

52122620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106185042-C-T

52122639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106185023-C-T

52122640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106185022-C-T

52122704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106184975-G-A

52123040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106184725-A-G

52123085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106184685-G-A

52123127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106184646-C-T

52123490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106183955-T-G

52123962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106183504-G-A

52123962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106183504-G-C

52124004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106183462-C-T

52124129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106183349-C-G

52124306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106183215-C-T

http://identifiers.org/hco/3/GRCh38#52124371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106183144-C-A

52124405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106183108-G-A

52124406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106183107-G-A

52125286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106182257-G-A

52125286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106182257-G-T

52125688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106181924-G-A

52125885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106181716-C-G

52125904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106181697-G-A

52125904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106181697-G-C

52126063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106181543-G-C

52126313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106181196-C-T

52127217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106180743-C-T

52128071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106180445-T-C

52128401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106180109-C-G

52128677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106179788-C-T

52128721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106179716-C-G

52128818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106179633-T-A

52128818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106179633-T-C

52128843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106179621-T-C

52128905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106179561-A-G

52129393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106179428-G-A

52129419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106179402-A-G

52129431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106179385-G-A

52129525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106179302-T-C

52129839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106178994-C-G

52130238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106178510-A-G

52130716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106178114-A-G

52131383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106177563-C-T

http://identifiers.org/hco/3/GRCh38#52133559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106176192-A-C

http://identifiers.org/hco/3/GRCh38#52133882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106175864-A-C

52133953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106175792-T-C

52133964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106175781-T-C

52134025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106175732-G-A

52134069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106175693-G-A

52134719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106175562-G-A

52134819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106175496-T-A

52134819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106175496-T-C

52134819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106175496-T-G

52134839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106175476-T-C

52134927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106175397-T-C

52135082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106175275-T-G

52135149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106175195-C-G

52135149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106175195-C-T

52135478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106174841-G-C

52135917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106174398-G-C

52136082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106174248-G-A

52136082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106174248-G-C

http://identifiers.org/hco/3/GRCh38#52136170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106174165-A-C

52136335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106174006-T-A

http://identifiers.org/hco/3/GRCh38#52137019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106173570-A-C

52137079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106173529-G-A

52137367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106173273-T-A

52137657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106172965-G-A

52137809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106172837-C-T

52137917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106172740-A-G

52138028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106172671-G-A

52138028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106172671-G-T

52138331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106172309-G-C

52138331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106172309-G-T

52138393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106172247-A-G

http://identifiers.org/hco/3/GRCh38#52138431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106172210-C-A

52138431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106172210-C-T

52139448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106171645-C-T

52139583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106171533-C-T

52139624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106171492-C-T

52139669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106171470-G-C

http://identifiers.org/hco/3/GRCh38#52139953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106171190-A-C

52140072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106171073-G-C

52140072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106171073-G-T

52140448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106170742-A-T

52140840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106170388-G-A

52140840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106170388-G-C

52140840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106170388-G-T

52140899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106170330-G-A

52140915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106170316-T-C

52140969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106170260-G-A

http://identifiers.org/hco/3/GRCh38#52141155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106170099-C-A

52141228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106170026-C-G

52141231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106170023-A-G

52141404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106169843-C-G

52141481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106169762-G-T

52141571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106169676-T-C

52141573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106169674-C-T

52141932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106168466-T-C

52141955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106168443-A-G

52142017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106168382-G-A

52142125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106168276-C-T

52142127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106168274-G-A

52142127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106168274-G-C

52142427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106167967-G-A

52142427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106167967-G-T

52142518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106167891-T-C

52142518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106167891-T-G

52143184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106167310-A-G

52143317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106167180-T-A

52143653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106166975-C-T

http://identifiers.org/hco/3/GRCh38#52143763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106166872-C-A

52143974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106166673-C-T

52144263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106166458-G-T

52144534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106166174-G-A

52144534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106166174-G-C

52145328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106165751-T-A

52145725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106165428-G-T

http://identifiers.org/hco/3/GRCh38#52145750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106165403-C-A

52145750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106165403-C-T

http://identifiers.org/hco/3/GRCh38#52145756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106165396-C-A

52145798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106165352-A-G

52145814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106165335-C-T

52145820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106165329-G-A

52145820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106165329-G-T

52145908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106165241-C-T

52145975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106165175-G-A

52145975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106165175-G-T

52146199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164776-G-A

52146212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164761-A-G

52146296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164696-G-A

http://identifiers.org/hco/3/GRCh38#52146840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106164230-C-A

52146840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164230-C-G

52146840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164230-C-T

http://identifiers.org/hco/3/GRCh38#52146842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106164228-C-A

52146842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164228-C-G

52146842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164228-C-T

52146843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164227-G-A

52146843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164227-G-C

52146843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164227-G-T

52146864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164206-G-A

52146864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164206-G-T

52146919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164144-C-T

52146961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164107-G-A

52146961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164107-G-C

52146961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106164107-G-T

52147109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106163963-G-A

52147109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106163963-G-T

52147120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106163952-C-T

52148279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106163758-T-A

http://identifiers.org/hco/3/GRCh38#52148288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106163767-C-A

52148929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106163281-G-A

http://identifiers.org/hco/3/GRCh38#52149080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106163129-C-A

52149080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106163129-C-G

52149089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106163120-A-G

52149141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162832-T-C

52149228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106162751-T-C

52149404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162575-A-G

52149462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162520-C-G

52149463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162519-T-C

52149463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162519-T-G

http://identifiers.org/hco/3/GRCh38#52149480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106162512-C-A

52149480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162512-C-T

http://identifiers.org/hco/3/GRCh38#52149502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106162501-C-A

52149502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162501-C-T

http://identifiers.org/hco/3/GRCh38#52149509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106162494-C-A

52149509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162494-C-T

http://identifiers.org/hco/3/GRCh38#52149510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106162493-C-A

52149554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162447-A-G

52149704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162358-A-G

http://identifiers.org/hco/3/GRCh38#52149778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106162285-C-A

http://identifiers.org/hco/3/GRCh38#52149785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106162278-C-A

http://identifiers.org/hco/3/GRCh38#52149789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106162274-C-A

52149789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162274-C-G

52149789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162274-C-T

52149803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162262-G-C

52149873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106162192-C-T

52149915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106162150-C-T

52149917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106162148-A-T

52149930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106162135-G-A

http://identifiers.org/hco/3/GRCh38#52149941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106162124-C-A

52149941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106162124-C-T

52149942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106162123-G-A

52149942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106162123-G-C

52149942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106162123-G-T

http://identifiers.org/hco/3/GRCh38#52150072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106162008-C-A

52150072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162008-C-G

http://identifiers.org/hco/3/GRCh38#52150137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106161943-C-A

52150539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106160911-A-G

http://identifiers.org/hco/3/GRCh38#52150625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106160847-C-A

52150625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106160847-C-T

52150643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106160826-T-C

52150643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106160826-T-G

52150645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106160824-T-A

52150647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106160822-C-T

52150927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106160211-G-A

52150927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106160211-G-T

52150932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106160205-G-A

52150932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106160205-G-T

http://identifiers.org/hco/3/GRCh38#52150933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106160204-C-A

52150933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106160204-C-T

52150935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106160202-T-G

52151130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106160005-A-G

52151139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106160000-G-A

52151185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106159957-G-A

52151185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106159957-G-T

52151192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106159954-G-A

52151192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106159954-G-C

52151192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106159954-G-T

52151221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106159925-T-C

52151224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106159922-A-G

52151473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106159777-T-C

52153326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106159549-G-A

52153554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106159315-T-A

http://identifiers.org/hco/3/GRCh38#52153642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106159235-C-A

52153755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106159153-G-T

52153954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106158985-C-G

52153974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106158965-C-T

52154082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106158877-G-C

52154163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106158796-C-T

52154220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106158754-T-A

52154220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106158754-T-C

52154371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: 106158637-A-G

52154373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106158635-G-A

52154373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106158635-G-T

http://identifiers.org/hco/3/GRCh38#52154380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106158628-C-A

52154380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106158628-C-G

52154380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106158628-C-T

52154383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106158625-G-A

52154383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106158625-G-C

52154383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106158625-G-T

52154395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106158587-G-A

52154395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106158587-G-T

http://identifiers.org/hco/3/GRCh38#52154457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#106158526-C-A

52154457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106158526-C-G

52154504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106158479-G-A

52154504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106158479-G-T

52154524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106158459-G-A

52154524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106158459-G-C

52154524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106158459-G-T

52154529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106158454-G-A

52154529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106158454-G-T

52154532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106158451-G-A

52154532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106158451-G-T

http://identifiers.org/hco/3/GRCh38#52154554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#106158429-C-A

52154554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106158429-C-G

52154554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106158429-C-T

http://identifiers.org/hco/3/GRCh38#52154616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106158378-A-C

52154616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5 prime UTR variant
orthologous variants: 106158378-A-G

http://identifiers.org/hco/3/GRCh38#52154662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#106158327-C-A

52154666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24488
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106158323-G-T