33376316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 5 prime UTR variant
orthologous variants: 104240786-T-A

33376459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 5 prime UTR variant
orthologous variants: 104240694-G-A

http://identifiers.org/hco/11/GRCh38#33376683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#104240475-C-A

33376696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: synonymous variant
orthologous variants: 104240462-G-A

33376696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: synonymous variant
orthologous variants: 104240462-G-T

33376760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104240398-G-A

33376760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104240398-G-T

http://identifiers.org/hco/11/GRCh38#33376916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104240242-C-A

33377678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104239512-C-T

http://identifiers.org/hco/11/GRCh38#33377704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104239484-A-C

33378311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104238923-C-G

33378321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104238913-C-T

33378416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104238817-G-T

33378577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104238662-A-T

33378648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104238604-A-G

http://identifiers.org/hco/11/GRCh38#33378868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104238394-A-C

33379010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104238258-G-A

33379225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104238024-G-A

33379796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104237508-A-G

33379876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104237431-T-C

33379926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104237381-G-C

33380119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104237196-A-T

33381052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104236684-A-G

33381070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104236670-G-A

33381099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104236641-G-A

33381099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104236641-G-T

33383086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104235133-A-G

33383140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104235088-G-T

33383617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104234658-G-A

33383763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104234554-C-T

33383940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104234410-A-G

33383982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104234352-G-A

33384092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104234077-G-C

33384300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104233910-C-T

33384402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104233806-A-G

33384925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104233330-A-G

33384925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104233330-A-T

33385820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104232351-T-C

33385881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104232292-T-C

33385952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104232014-T-C

33385963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104232003-T-C

http://identifiers.org/hco/11/GRCh38#33387747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104230153-C-A

33389710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104228546-A-G

33390313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104227979-C-G

33390378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104227922-C-T

33390702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104227630-A-G

33391047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104227102-A-G

33391357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104226815-C-T

33391417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104226762-G-T

http://identifiers.org/hco/11/GRCh38#33391603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104226589-C-A

33391603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104226589-C-G

33391670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104226522-G-T

33391708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104226481-C-G

33391708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104226481-C-T

33393136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104224711-C-T

33393172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104224675-G-A

33393200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104224645-C-T

33393854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104224221-C-T

33393969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104224111-T-A

33394017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104224064-G-T

33394402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104223692-T-C

33394607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104223491-G-A

33394848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104223280-A-G

33394853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104223275-T-C

33395411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104223040-T-C

33395465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104222986-T-C

33395465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104222986-T-G

33395681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104222924-T-C

33395935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104222666-C-T

33396204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104222411-A-G

33398321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104220850-A-G

33398363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104220820-T-A

http://identifiers.org/hco/11/GRCh38#33398399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104220784-C-A

33398399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104220784-C-G

33398399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104220784-C-T

33398710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104220491-T-C

http://identifiers.org/hco/11/GRCh38#33398794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104220408-C-A

33399631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104219793-C-T

http://identifiers.org/hco/11/GRCh38#33399732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104219691-C-A

33400329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104218750-G-A

33400363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104218206-T-G

33400399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104218172-T-A

33400506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104218064-G-A

33400549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104218028-A-G

33400780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104217630-A-G

33400826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104217589-T-G

http://identifiers.org/hco/11/GRCh38#33402556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104212503-A-C

http://identifiers.org/hco/11/GRCh38#33402728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104212337-C-A

33402728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104212337-C-G

33402728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104212337-C-T

33403118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104211930-T-C

33403123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104211925-T-C

http://identifiers.org/hco/11/GRCh38#33403166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104211880-C-A

33403790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104211754-C-T

33403864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104211690-A-T

33403914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104211641-G-A

33403914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104211641-G-T

33403928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104211634-G-A

33405131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104210951-C-T

33405182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104210899-A-G

33405471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104210377-A-G

33405948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104210280-T-C

33406045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104210191-T-C

33406045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104210191-T-G

33406346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104209866-T-C

33406348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104209864-C-T

33406376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104209836-G-A

33406481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104209733-C-T

33406921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104209306-T-C

33407066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104209155-C-T

33408614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104207046-T-C

http://identifiers.org/hco/11/GRCh38#33409299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104206525-A-C

http://identifiers.org/hco/11/GRCh38#33409378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104206451-A-C

33409698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104205425-A-G

33409718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104205402-A-G

33409784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104205348-T-C

33409805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104205327-C-T

33410065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104205036-C-T

33410078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104205021-T-A

33410096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104205003-G-A

33410343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104204767-T-A

33410468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104204663-C-T

33410486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104204646-A-G

33411027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104204189-G-A

33411094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104204135-T-C

33411234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104203807-T-C

33411375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104203683-T-C

33411461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104203595-G-A

33412659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104201487-C-T

33412813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104201355-G-A

33412868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104201292-A-G

33413175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104200631-C-G

33413227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104200579-T-C

33413584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104200166-C-T

http://identifiers.org/hco/11/GRCh38#33414012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104199835-A-C

33414365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104199470-A-G

33414540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104199306-C-T

33414608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104199241-A-G

33416438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104198002-C-T

33416762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104197934-G-A

33416846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104197862-T-C

33416897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104197811-T-A

33416959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104197749-A-G

33417640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104197019-G-A

33418191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104196008-G-T

33418814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104195465-C-T

http://identifiers.org/hco/11/GRCh38#33418856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104195414-C-A

33418883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104195384-A-G

33418883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104195384-A-T

33418903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104195357-T-G

33419071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104195231-T-C

33419351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104194996-C-G

33419452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104194905-G-A

33419518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104194837-T-C

33419530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104194825-T-C

33420011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104194704-G-A

33420072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104194647-A-G

http://identifiers.org/hco/11/GRCh38#33420161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104194557-A-C

33420186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104194533-C-G

33420186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104194533-C-T

http://identifiers.org/hco/11/GRCh38#33420206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104194513-C-A

33420206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104194513-C-T

33420207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104194512-T-G

33420781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104193954-A-G

33420958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104193764-C-T

http://identifiers.org/hco/11/GRCh38#33420961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104193761-C-A

http://identifiers.org/hco/11/GRCh38#33420966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104193756-A-C

http://identifiers.org/hco/11/GRCh38#33421474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104193284-C-A

33421474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104193284-C-T

33421520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104193239-T-C

http://identifiers.org/hco/11/GRCh38#33421538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104193222-A-C

http://identifiers.org/hco/11/GRCh38#33421627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104193141-A-C

33421636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104193132-A-G

33422653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104192857-A-G

33422702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104192817-T-G

33422705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104192814-T-A

33422781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104192753-G-C

33422782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104192752-C-T

33422831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104192384-G-C

33424701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104191690-C-T

33425319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104191090-A-T

33425350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104191066-T-G

33425886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104190575-T-C

33425981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104190492-A-G

33426078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104190404-C-T

http://identifiers.org/hco/11/GRCh38#33426370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104190107-C-A

33426370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104190107-C-T

33426489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104189988-C-G

33426490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104189987-C-T

33426531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104189959-G-A

33426548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104189945-G-A

33426749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104189753-C-G

33426850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104189622-C-T

33427186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104189346-T-C

33427187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104189345-C-G

33427253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104189275-A-G

33429513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104188303-T-A

33429533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104188288-C-T

33429601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104188210-T-C

33429869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104187882-T-C

http://identifiers.org/hco/11/GRCh38#33430230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104187234-A-C

33430230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104187234-A-T

33430238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104187226-C-T

33430605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104186849-C-T

33430715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104186746-C-G

33430764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104186696-G-A

33430764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104186696-G-C

33430812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104186651-A-G

http://identifiers.org/hco/11/GRCh38#33432594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104186383-A-C

33435044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104186152-T-G

33435263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104185951-A-G

33435310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104185904-T-G

33435328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104185885-G-A

33436476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104184810-C-T

http://identifiers.org/hco/11/GRCh38#33436546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104184758-C-A

33436546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104184758-C-T

http://identifiers.org/hco/11/GRCh38#33436547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104184757-A-C

33436547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104184757-A-G

33436618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104184686-A-G

33436959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104184377-T-A

33437540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104183830-A-G

33437698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104183682-G-A

33437774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104183603-C-T

33437846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104183531-A-G

33444600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104182599-T-C

33444683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104182508-T-C

33444769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104182431-C-G

33444820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104182386-C-T

33444822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104182384-C-T

33444823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104182383-G-A

33444823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104182383-G-C

33444943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104182284-G-A

33444956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104182271-C-T

33445227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104182031-C-T

33445294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104181964-A-G

33445311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104181946-T-C

33445329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104181928-T-G

33445425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104181832-A-T

33447082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104179329-C-G

33447234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104179224-T-C

http://identifiers.org/hco/11/GRCh38#33447323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104179141-C-A

33447583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104178608-C-G

33447606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104178592-T-C

33447623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104178575-G-A

33447751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104178462-C-G

http://identifiers.org/hco/11/GRCh38#33447890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104178367-A-C

33448368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104176415-A-G

33448565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104175942-A-G

33448584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104175924-A-G

33448584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104175924-A-T

33448654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104175862-C-T

http://identifiers.org/hco/11/GRCh38#33448797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104175715-C-A

33448846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104175678-A-T

33449191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104175073-T-C

33449191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104175073-T-G

33449220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104175045-A-G

33449265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104174988-A-T

33449267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104174986-T-C

http://identifiers.org/hco/11/GRCh38#33449336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104174923-A-C

33449841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104174444-G-A

33449965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104174274-A-G

33450136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104174099-T-C

33450517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104173732-G-A

33450517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104173732-G-T

33450524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104173725-C-T

http://identifiers.org/hco/11/GRCh38#33450614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104173680-C-A

33450628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104173666-T-C

33450643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104173651-A-G

33450643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104173651-A-T

33450970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104173375-C-T

http://identifiers.org/hco/11/GRCh38#33450983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104173362-C-A

33450983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104173362-C-T

http://identifiers.org/hco/11/GRCh38#33451043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104173310-C-A

33451043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104173310-C-T

33451214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104173114-T-G

33451267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104173064-A-G

33451268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104173063-T-G

33451272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104173059-T-A

33451370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104172960-T-C

33451399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104172933-G-A

33451430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104172902-C-T

33451479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104172853-T-C

33451479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104172853-T-G

33451715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104172632-A-G

33451853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104172489-G-T

33451855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104172487-T-C

33451908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104172415-A-G

33451908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104172415-A-T

33451968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104172357-G-T

33452009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104172316-T-G

33452125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104172176-C-T

http://identifiers.org/hco/11/GRCh38#33452151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104172145-C-A

33452831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104171477-C-G

33453092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104169193-A-G

33453247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104169034-A-T

33453332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104168938-G-A

33453563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104168766-C-T

http://identifiers.org/hco/11/GRCh38#33454307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104167906-A-C

33454307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104167906-A-G

33454400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104167818-C-G

33454759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104167479-G-A

33455163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104167419-G-C

33455177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104167405-C-T

33455270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104167313-G-A

33455455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104167127-G-A

33455534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104167031-G-A

33455761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104166871-A-G

33455917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104166738-A-G

33456276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104166380-G-A

33458888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104165829-T-A

33459118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104165635-T-C

http://identifiers.org/hco/11/GRCh38#33459134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104165619-C-A

33459134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104165619-C-T

33459257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104165469-G-C

33459283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104165446-G-T

33459318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104165333-G-A

33460150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104164813-G-A

33460374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104164600-A-G

33460787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104164197-C-G

33460820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104164174-G-C

33461081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104163934-T-A

33461087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104163928-A-T

33461166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104163858-G-T

33461289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104163749-G-A

33461428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104163618-C-T

33461443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104163603-T-A

33461846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104163223-C-T

33461904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104163175-A-G

33462021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104163054-T-C

33462071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104163004-T-C

33462180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104162914-A-G

33462439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104162695-T-C

33462592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104162541-C-T

33463361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104161719-T-C

33463382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104161709-T-C

33463509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104161574-A-G

33463542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104161544-A-G

33463718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104161367-A-T

33463915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104160952-C-T

33463933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104160934-C-T

33463942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104160925-C-G

33464056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104160823-T-A

http://identifiers.org/hco/11/GRCh38#33464098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104160761-A-C

33464263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104160394-T-C

33464281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104160376-G-A

33464449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104160218-C-G

33464482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104160193-G-A

33464483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104160192-T-C

http://identifiers.org/hco/11/GRCh38#33464538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104160137-A-C

33464613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104160087-A-G

33464620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104160080-A-G

33464697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104160036-T-C

33464821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104159915-C-T

33464840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104159896-C-G

33464898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104159822-A-G

http://identifiers.org/hco/11/GRCh38#33464947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104159766-A-C

33465014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104159700-C-T

33467636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104158849-T-C

33467646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104158840-A-G

http://identifiers.org/hco/11/GRCh38#33467754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104158444-A-C

33467895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104158305-A-G

33468249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104157965-A-T

33468349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104157881-A-G

33468379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104157849-A-G

33468779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104157433-C-G

33469175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104156599-T-C

33469356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104156468-T-A

33469364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104156460-T-G

33469402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104156424-G-A

33469412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104156406-T-A

33469563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104156252-G-A

33469847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104155987-G-A

http://identifiers.org/hco/11/GRCh38#33473664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104154173-A-C

33474464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104153844-A-G

33474625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104153731-G-A

33475187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104153200-A-G

33475322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104153050-A-G

33476030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104152190-A-G

33476083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104152133-G-A

33476083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104152133-G-C

33476251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104151974-A-G

33476280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104151949-G-A

33476450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104151796-G-C

33476589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104151655-C-G

33476589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104151655-C-T

http://identifiers.org/hco/11/GRCh38#33476968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104151270-A-C

http://identifiers.org/hco/11/GRCh38#33477055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104150971-A-C

33477113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104150917-T-G

33477130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104150900-T-C

33477155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104150866-C-T

http://identifiers.org/hco/11/GRCh38#33477544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104150500-A-C

33477544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104150500-A-G

33477599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104150456-G-A

33477599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104150456-G-T

33477757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104150310-C-T

33478019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104149821-G-C

http://identifiers.org/hco/11/GRCh38#33478499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104149355-C-A

33479197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104148928-A-G

33479217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104148909-G-C

33479808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104148347-G-T

33479837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104148318-C-T

33479842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104148313-A-G

33479877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104148280-C-T

33480119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104148060-C-T

http://identifiers.org/hco/11/GRCh38#33480126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104148053-A-C

33480330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104147839-C-T

33480536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104147257-T-C

33480597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104147201-A-G

33480699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104147116-G-T

33480704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104147111-C-G

33480759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104147070-C-G

33483999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104145990-G-C

33484005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104145984-A-G

33484263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104145594-A-G

33484495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104145401-G-A

33484532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104145360-C-T

33484642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104145281-G-A

33484757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104144832-C-T

33484877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104144713-G-T

33484925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104144666-C-G

33486616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104144176-T-C

33486629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104144163-A-G

33487271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104143510-T-C

33487353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104143429-C-T

33487397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104143386-T-C

33487481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104143334-A-G

33487600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104143230-C-T

33487692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104143136-T-C

33489527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104141197-A-G

33489628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104141074-G-A

33490268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104140513-C-G

33490345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104140481-A-G

33490345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104140481-A-T

33490964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104140115-A-G

33490980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104140093-C-G

33491012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104140067-T-G

33491047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104140032-A-G

33491344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104139772-A-G

33491582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104139597-T-A

http://identifiers.org/hco/11/GRCh38#33491590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104139589-C-A

33491606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104139573-T-A

33491662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104139368-A-G

33492059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104138893-G-A

33492091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104138867-T-G

33492119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104138839-C-T

33492154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104138804-G-A

33492419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104138552-G-T

33492426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104138545-A-G

33492725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104138264-T-A

33492727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104138262-A-G

33492884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104138107-C-T

33493567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104137743-G-C

33493812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104137516-A-G

33493822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104137506-T-G

33493849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104137482-G-A

33493877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104137455-G-A

33494154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104136676-A-G

33494232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104136601-A-T

33494238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104136595-T-A

33494238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104136595-T-C

33494346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104136473-G-C

33494367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104136452-A-T

33494722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104136136-A-G

33494759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104136100-G-A

33494932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104135930-C-T

33496272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104135751-G-A

33496392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104135619-G-A

33496392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104135619-G-C

33496392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104135619-G-T

33496549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104135465-A-G

33496580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104135434-T-C

33496592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104135424-A-G

33496614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104135398-T-C

33496617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104135395-A-G

33497042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104134925-C-T

33497043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104134924-T-C

33497316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104134563-A-G

33497397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104134485-A-G

33497446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104134439-C-T

33497453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104134432-G-A

33497649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104134123-G-A

33497649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104134123-G-T

33498556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104132969-C-T

33499065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104132079-A-G

33499076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104132068-C-G

33500807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104129864-A-G

33501107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104129659-A-T

33501191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104129573-A-G

33501324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104129448-G-A

33501328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104129444-C-T

33501417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104129356-G-T

33502052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104128763-A-G

33502355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104128481-A-G

33502378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104128458-C-T

33502542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104128369-T-C

33502574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104128337-G-C

33503815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104127324-A-G

33503842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104127297-C-T

33503920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104127237-G-A

33503920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104127237-G-C

33505180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104126910-A-G

33505215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104126874-A-G

33505217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104126872-A-G

33505260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104126825-A-G

33505355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104126731-A-G

33505393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104126697-C-G

33505506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104126599-A-G

33505693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104126280-C-G

33505875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104126128-G-A

33506016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104125782-A-G

http://identifiers.org/hco/11/GRCh38#33506179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104125636-A-C

33506795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104125249-A-G

33506826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104125217-G-A

33507217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104124858-G-A

33507225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104124850-C-G

33507733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104121843-G-C

33508326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104121240-T-G

33508472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104121098-G-A

33508603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104120966-T-G

33508688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104120879-A-T

33508914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104120654-G-A

33509341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104120155-T-G

http://identifiers.org/hco/11/GRCh38#33509375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104120120-C-A

33509461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104120034-G-A

33509767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104119728-T-C

33510523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104119354-G-C

33510948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104119092-G-C

33511252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104118617-C-T

33511325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104118538-G-A

33511530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104118353-G-A

33511690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104118116-A-G

33511789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104118024-C-G

33513112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104117349-C-T

33513299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104117128-G-A

33514379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104116445-C-G

33514424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104116400-C-T

33514441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104116383-A-T

33514487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104115966-A-G

33514542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104115909-A-G

33514792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104115655-G-C

33514827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104115629-G-A

33514880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104115578-A-G

33516601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104114688-G-A

http://identifiers.org/hco/11/GRCh38#33517078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104113896-A-C

33518588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104113350-G-A

33519885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104112367-G-T

33519930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104112327-T-C

33520785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104111433-T-C

33521541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104110414-G-A

33522603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104109266-A-G

33522632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104109217-A-G

http://identifiers.org/hco/11/GRCh38#33523046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104108799-A-C

33523082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104108768-G-A

33523326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104108490-T-C

33523424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104108387-T-A

33524818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: -G-C

33524833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: -T-A

33524833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: -T-G

33530816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104106728-T-C

33530863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104106682-C-T

33531555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104106040-C-T

33531567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104106028-A-T

33531603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104105992-A-G

33531801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104105778-G-A

33531939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104105639-A-G

33531940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104105638-A-G

33532060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104105518-C-T

33532063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104105514-C-T

http://identifiers.org/hco/11/GRCh38#33532463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104102775-C-A

33532463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104102775-C-G

33532463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104102775-C-T

33532674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104102587-G-A

33532754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104102513-G-A

33532882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104102412-C-G

33532889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104102383-C-T

33532958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104102318-A-G

33534579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104100821-C-T

33534623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104100775-G-A

33534634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104100764-A-G

33534641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104100757-T-C

33534730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104100687-T-C

33534840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104100574-A-G

33536010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104098069-A-G

33536097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104097997-T-C

http://identifiers.org/hco/11/GRCh38#33536133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104097961-C-A

http://identifiers.org/hco/11/GRCh38#33536186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104097908-A-C

33536628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104097504-A-G

33536728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104097401-A-G

33536749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104097380-A-G

33536945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104097205-C-T

33537161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104096782-T-C

33537240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104096730-A-G

33537273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104096671-G-T

33537322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104096617-G-A

33537322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104096617-G-C

33537674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104096295-C-T

33538508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104095561-A-G

33539109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104092591-A-G

33539735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104092175-G-C

33539939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104091975-A-G

http://identifiers.org/hco/11/GRCh38#33540027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104091904-C-A

33540124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104091814-C-T

33540198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104091765-G-A

33540337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104091641-A-G

33540501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104091507-G-A

33540611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104091411-A-T

33540875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104091191-A-G

33541061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104089667-T-C

33541147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104089578-T-C

33541325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104089389-G-A

33541472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104089292-A-G

33541507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104089259-C-T

http://identifiers.org/hco/11/GRCh38#33541679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104088980-C-A

33541679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104088980-C-T

33541702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104088944-G-A

33541702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104088944-G-T

33541706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104088940-G-C

33541706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104088940-G-T

33541717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104088929-G-A

33541717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104088929-G-T

33541964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104088689-T-C

33541964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104088689-T-G

33542014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104088639-G-A

http://identifiers.org/hco/11/GRCh38#33542084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104088569-A-C

33542084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104088569-A-G

http://identifiers.org/hco/11/GRCh38#33542187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104088466-C-A

33542220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 104088436-A-G

http://identifiers.org/hco/11/GRCh38#33542263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104088396-C-A

http://identifiers.org/hco/11/GRCh38#33542303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104088356-C-A

33542303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104088356-C-T

http://identifiers.org/hco/11/GRCh38#33542348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104088308-A-C

33542348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 104088308-A-G

33542403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 104088253-C-T

33542588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104088068-C-T

33542613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104088043-A-T

33542726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104087939-A-G

http://identifiers.org/hco/11/GRCh38#33542730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104087935-C-A

33542735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104087930-C-G

33542735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104087930-C-T

33542754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 104087911-G-A

33542755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104087910-C-T

http://identifiers.org/hco/11/GRCh38#33542790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104087875-A-C

33542790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 104087875-A-G

33543140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 104087525-T-C

33543531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 104087149-G-A

33543552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 104087128-T-G

33543603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 104087077-T-C

33543682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104086998-C-T

33543772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104086908-C-G

33543783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 104086897-A-G

33543837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104086843-T-A

33543946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104086734-G-A

33543946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104086734-G-T

33544040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104086646-G-A

33544048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104086638-G-A

33544261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104086434-T-A

33544261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104086434-T-C

33544261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104086434-T-G

33544587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104086093-C-G

33544688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104085991-G-A

33544688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104085991-G-T

33544714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104085966-G-A

33544878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104085787-G-A

33544944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104085733-A-G

33545099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: synonymous variant
orthologous variants: 104085578-T-C

33545249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104085428-C-T

33545261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: synonymous variant
orthologous variants: 104085416-T-C

33545261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104085416-T-G

http://identifiers.org/hco/11/GRCh38#33545453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104085233-C-A

http://identifiers.org/hco/11/GRCh38#33545460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104085226-C-A

33545460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104085226-C-T

http://identifiers.org/hco/11/GRCh38#33545461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104085225-C-A

33545461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104085225-C-T

33545550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104085144-T-A

33545550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104085144-T-C

33545664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104084669-T-C

33545725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104084614-T-C

33545745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104084594-A-G

33545815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104084511-A-G

33545842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104084484-G-T

33546022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104084330-A-G

33547078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104083659-T-C

33547382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104083419-A-G

http://identifiers.org/hco/11/GRCh38#33547442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104083355-A-C

33547509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104083268-C-T

33547525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104083252-G-A

33547748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104083066-C-T

33547781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104083033-A-G

33547796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104083018-A-G

33547865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104082949-G-A

33547865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104082949-G-C

http://identifiers.org/hco/11/GRCh38#33547877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104082937-C-A

33547913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104082903-T-A

33547913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104082903-T-C

33547936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104082882-G-A

33547943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104082875-T-C

33548358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104082497-C-G

33548358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104082497-C-T

33549066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104081894-A-G

33549072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104081888-C-G

33549141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104081817-A-G

33549143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104081815-G-A

33549143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104081815-G-T

33549185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104081776-A-T

33549212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104081733-T-C

33549340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104081599-T-A

33549345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104081594-C-T

33549463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104081460-A-G

33549569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104081372-G-A

http://identifiers.org/hco/11/GRCh38#33549675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104081207-A-C

33549676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104081206-T-C

http://identifiers.org/hco/11/GRCh38#33549685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104081197-A-C

33549691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104081191-A-G

33549767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104081121-G-A

33550320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104080570-T-C

33550459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104080491-A-G

http://identifiers.org/hco/11/GRCh38#33550467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104080483-C-A

33550467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104080483-C-G

33550467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104080483-C-T

33550474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104080476-G-T

33550506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104080445-C-T

http://identifiers.org/hco/11/GRCh38#33550523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104080427-C-A

33550822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104079979-A-G

33550877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104079870-C-T

33551023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104079733-G-A

http://identifiers.org/hco/11/GRCh38#33551229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104079527-C-A

33551461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104079320-A-G

33551522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104079261-A-G

33551663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104079146-T-A

33551949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104078889-C-G

http://identifiers.org/hco/11/GRCh38#33552127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104078710-A-C

33552127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: synonymous variant
orthologous variants: 104078710-A-G

33552185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104078652-G-A

33552258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104078580-T-C

33552258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104078580-T-G

33552290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104078551-G-A

33552299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104078542-G-A

33552299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104078542-G-T

33552370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104078449-G-T

http://identifiers.org/hco/11/GRCh38#33552380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104078439-C-A

33552380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104078439-C-T

33552700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104077976-A-G

33552779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104077910-A-G

33553451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104077477-A-T

33553651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104077254-G-C

33553786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104077138-A-G

33553906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104077031-A-G

33554112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104076844-C-T

33554300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104076667-G-A

33554300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104076667-G-T

http://identifiers.org/hco/11/GRCh38#33554412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104076572-A-C

33554412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104076572-A-T

33555308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104075212-A-G

33555326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104075194-G-T

33555369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104075151-A-G

33555645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104074900-A-G

http://identifiers.org/hco/11/GRCh38#33555660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104074886-C-A

33555699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104074847-C-T

33555768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104074798-G-C

33555774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104074792-A-G

33555777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104074790-C-T

http://identifiers.org/hco/11/GRCh38#33555840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104074722-A-C

33555920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104074659-T-C

33556248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104074304-G-A

http://identifiers.org/hco/11/GRCh38#33556281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104074271-A-C

33556281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104074271-A-G

33556324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104074228-T-C

33556579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104074039-A-G

33556634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104073980-G-T

33556839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104073806-A-G

33557332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104073553-A-G

33557363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104073515-T-A

33558507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104072766-G-A

33558552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104072731-G-A

33558562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104072724-G-A

33558675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104072619-T-C

33558728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104072561-G-A

33558728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104072561-G-T

33559519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104071803-G-A

33559668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104071658-T-C

33559902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104071426-A-G

33560259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104071186-A-G

33560492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104071016-G-T

33560530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104070987-C-G

33560581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104070939-T-C

33560608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104070912-A-T

33560759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104070763-C-T

33561220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104069332-G-A

33561356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104069211-G-A

33561639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104069090-T-C

33561782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104068954-T-C

33561848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104068893-A-G

http://identifiers.org/hco/11/GRCh38#33562094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104068667-A-C

33562124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104068640-G-A

33562153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104068619-A-G

33562163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104068606-G-T

33562336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104068421-T-A

33562493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104068353-G-C

33562559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104068290-C-G

33562559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104068290-C-T

33563460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104068018-T-C

33563460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104068018-T-G

33563500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104067984-C-T

33563518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104067967-C-T

http://identifiers.org/hco/11/GRCh38#33563521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104067964-C-A

33563521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104067964-C-T

33563686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104067779-A-G

33563736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104067709-A-G

33563889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104067566-T-C

33563910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104067544-T-C

33564176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104067285-A-T

http://identifiers.org/hco/11/GRCh38#33564283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104067184-C-A

33564771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104066603-T-C

33564810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104066570-C-T

33564852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104066529-A-G

33564930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104066455-T-C

http://identifiers.org/hco/11/GRCh38#33565172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104066270-A-C

33565172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104066270-A-G

33565283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104066166-T-G

33565332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104066117-C-T

33566056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104065802-A-G

33566177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104065688-T-C

http://identifiers.org/hco/11/GRCh38#33566912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104065022-A-C

33566912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104065022-A-G

33567175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104064772-T-C

33567434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104064542-C-T

33567496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104064479-G-A

33567561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104064416-T-A

http://identifiers.org/hco/11/GRCh38#33567776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104064208-A-C

33567953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104064019-G-A

33567953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104064019-G-T

33567970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104064006-G-A

33567973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104064003-A-G

33567973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104064003-A-T

33568047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063937-A-G

33568065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063919-T-C

http://identifiers.org/hco/11/GRCh38#33568183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104063801-C-A

33568183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104063801-C-T

33568184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104063800-G-A

http://identifiers.org/hco/11/GRCh38#33568257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104063733-C-A

33568257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063733-C-G

33568257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063733-C-T

33568267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063722-G-C

33568267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063722-G-T

http://identifiers.org/hco/11/GRCh38#33568274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104063715-A-C

33568274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063715-A-G

33568274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063715-A-T

33568275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063714-G-A

33568275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063714-G-C

33568275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063714-G-T

33568285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063711-T-C

33568293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063703-G-T

33568320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063676-G-A

33568320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063676-G-T

33569272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063636-A-G

33569426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063516-G-A

33569751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104063258-A-G

33573309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104062353-T-G

33573371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104062287-A-G

http://identifiers.org/hco/11/GRCh38#33574170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104061337-C-A

33574189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104061324-T-A

33574476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104061049-G-C

33574622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104060874-G-A

http://identifiers.org/hco/11/GRCh38#33574631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104060865-C-A

33574631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104060865-C-T

33574850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104060650-A-G

33574888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104060616-T-C

33575043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104060465-A-T

33575929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104059683-A-G

33576251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104059360-T-C

33576299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104059319-T-A

33576317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104059302-C-T

33576356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104059259-G-A

33576356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104059259-G-T

33576360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104059255-G-T

33576527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104059098-A-T

33576708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104058945-G-A

33576716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104058937-C-T

33577100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104058601-G-A

33581066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104055569-T-C

33581068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104055567-G-A

33581200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104055463-T-C

http://identifiers.org/hco/11/GRCh38#33581226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104055436-A-C

http://identifiers.org/hco/11/GRCh38#33581393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104055302-C-A

33581393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104055302-C-T

33581775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104054943-C-T

33581942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104054764-A-T

33581952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104054712-A-G

33581978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104054686-T-C

33582187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104054438-G-A

33582198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104054427-A-G

http://identifiers.org/hco/11/GRCh38#33582787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104052389-A-C

33582839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104052345-G-A

33582941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104052245-C-T

33583199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104051765-G-A

33583199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104051765-G-T

33583269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104051691-T-G

http://identifiers.org/hco/11/GRCh38#33583325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104051654-C-A

33583325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104051654-C-G

33583515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104051467-G-T

33583538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104051445-G-T

33583591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104051388-G-A

33583591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104051388-G-T

33583703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104051280-A-G

33583988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104051042-T-C

33583990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104051040-G-A

33584039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104051004-C-T

33584256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104050786-C-T

http://identifiers.org/hco/11/GRCh38#33584260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104050782-C-A

http://identifiers.org/hco/11/GRCh38#33584447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104050467-A-C

33584619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104050297-T-C

33584652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104050264-G-C

33584758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104050166-G-A

33584811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104049548-T-G

33585650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104049036-A-G

http://identifiers.org/hco/11/GRCh38#33585985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104048726-A-C

33586159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104048586-T-C

33586340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104048403-G-T

http://identifiers.org/hco/11/GRCh38#33586651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104048233-A-C

33586669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104048218-C-G

33586808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104048152-A-G

33587082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104048087-G-A

33587082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104048087-G-C

33587091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104048076-G-A

33587323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104047754-T-A

33587323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104047754-T-C

33587635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104047460-A-G

33587766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104047333-G-A

http://identifiers.org/hco/11/GRCh38#33587829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104047272-A-C

33587952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104047159-G-A

33588223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104046886-G-A

33588410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104046700-A-G

33588440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104046674-T-C

33588482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104046641-T-C

33588732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104046440-C-T

33590486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104045524-T-C

33590512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104045498-G-A

33590620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104045395-C-T

33590720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104045301-G-T

33590760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104045261-G-A

http://identifiers.org/hco/11/GRCh38#33590797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104045224-A-C

33590908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104045126-T-C

33590992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104045043-A-G

33591029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104045007-A-G

33591029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104045007-A-T

33591042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104044994-C-T

33591043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104044993-T-C

http://identifiers.org/hco/11/GRCh38#33591151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104044703-C-A

33591204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104044651-A-G

http://identifiers.org/hco/11/GRCh38#33591209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104044646-C-A

33591209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104044646-C-G

33591209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104044646-C-T

33591213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104044642-T-C

33591270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104044585-C-G

33591366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104044489-G-A

33591366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104044489-G-T

33591382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104044473-G-A

33591416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant
orthologous variants: 104044439-G-C

http://identifiers.org/hco/11/GRCh38#33591427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104044428-C-A

33591427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104044428-C-G

33591427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104044428-C-T

33591435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104044421-T-C

http://identifiers.org/hco/11/GRCh38#33591493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104044390-C-A

33591493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104044390-C-G

33591493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104044390-C-T

33591712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104044176-T-C

http://identifiers.org/hco/11/GRCh38#33592004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104043770-A-C

http://identifiers.org/hco/11/GRCh38#33592268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104043525-C-A

33592268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104043525-C-T

33592291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104043507-T-G

33592387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104043416-T-C

33592497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104043335-T-C

33592575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104043265-G-A

33592826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104043114-A-G

33592907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104043032-A-G

33592910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104043024-G-A

33592980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104042951-G-A

33593071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104042862-A-G

33593093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104042840-G-T

33593490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104042783-T-C

33593573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104042696-G-A

http://identifiers.org/hco/11/GRCh38#33593621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104042671-A-C

33593691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104042624-T-C

33593702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104042612-G-C

33593718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104042596-G-A

33593890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104042465-C-T

33593908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104042447-T-C

33594002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104042349-C-G

33594017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104042334-A-T

33594121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104042256-A-G

33594484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104041942-C-G

33594778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104041678-C-T

33594790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104041666-G-A

33595116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104041352-A-G

http://identifiers.org/hco/11/GRCh38#33595695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104040781-A-C

33595846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104040635-A-G

33595862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104040615-G-T

33596011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104040460-G-A

33596073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104040401-G-A

33596933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104039856-C-T

33597141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104039647-G-T

33597744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104039440-T-C

33597804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104039398-A-T

33597855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104039376-G-A

33597855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104039376-G-T

33598074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104039180-A-G

33598232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104039054-G-C

33598578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104038822-A-G

http://identifiers.org/hco/11/GRCh38#33598713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104038658-C-A

http://identifiers.org/hco/11/GRCh38#33598722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104038649-A-C

33598725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104038646-G-T

33598944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 104038428-A-G

33598953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104038419-A-G

http://identifiers.org/hco/11/GRCh38#33598961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104038411-C-A

33598982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104038391-T-A

http://identifiers.org/hco/11/GRCh38#33599034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104038349-C-A

http://identifiers.org/hco/11/GRCh38#33599041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104038342-C-A

33599041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104038342-C-T

33599047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104038336-G-T

http://identifiers.org/hco/11/GRCh38#33599076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104038311-C-A

33599158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104038234-T-C

http://identifiers.org/hco/11/GRCh38#33599199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104038196-A-C

33599199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104038196-A-G

http://identifiers.org/hco/11/GRCh38#33599202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104038193-C-A

33599202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104038193-C-G

33599340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104038091-A-G

33599392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104038042-T-C

33599423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104038011-G-T

33601449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104037650-T-A

33601674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104037462-A-T

33601712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104037436-A-G

33601799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104037346-G-A

33601830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104037315-A-G

http://identifiers.org/hco/11/GRCh38#33605514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104036614-A-C

33606002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104036121-C-T

33606118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104035998-T-A

33606259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104035845-T-C

http://identifiers.org/hco/11/GRCh38#33606554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104035647-C-A

http://identifiers.org/hco/11/GRCh38#33606573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104035643-C-A

33606832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104035392-T-C

33606855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104035374-T-A

33606872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104035357-A-G

33606939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104035304-T-C

33607035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104035228-G-A

33607358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104034970-T-C

33607507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104034642-T-C

http://identifiers.org/hco/11/GRCh38#33607794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104033927-A-C

33607861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104033866-G-A

33608041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104033726-G-A

33608113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104033656-T-A

33608303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104033504-A-G

33608305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104033502-G-T

33608324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104033494-A-G

33609245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104032498-C-T

33609273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104032463-C-G

33609326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104032424-C-T

33609481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104032253-A-G

33609728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104031698-T-C

33609836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104031582-T-A

33609836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104031582-T-C

33609852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104031566-C-T

33609865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: synonymous variant
orthologous variants: 104031553-G-C

33609865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: synonymous variant
orthologous variants: 104031553-G-T

33609949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: synonymous variant
orthologous variants: 104031472-C-T

33609967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: undefined
orthologous variants: 104031454-G-A

http://identifiers.org/hco/11/GRCh38#33610032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104031387-C-A

33610123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104031307-C-T

33610155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104031275-G-A

33610209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104031223-T-C

33610242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104031190-G-C

33610354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104031081-C-T

http://identifiers.org/hco/11/GRCh38#33610487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104030953-C-A

33610517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104030926-G-C

33610703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104030750-C-T

33610911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104030540-G-A

http://identifiers.org/hco/11/GRCh38#33611018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104028898-C-A

33611149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104028769-T-C

33611474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104028460-C-T

33611563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104028380-A-G

33611658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104028287-A-G

33612269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104027828-T-C

33614276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104027184-T-C

33614276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104027184-T-G

33614348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104027117-G-A

33615103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104026661-A-G

33615232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104026526-G-T

33615950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104024933-T-C

33616134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104024752-G-A

33616360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104024550-T-C

33616360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104024550-T-G

33616502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104024401-C-T

33616581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104024318-C-T

33617602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104023693-G-C

33617612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104023683-G-A

33617612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104023683-G-T

33617703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104023607-A-G

33618015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104023433-C-T

33618036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104023413-A-G

http://identifiers.org/hco/11/GRCh38#33618182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104023250-C-A

33618235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104023199-G-A

33618383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104023051-G-A

33618582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104022858-C-T

http://identifiers.org/hco/11/GRCh38#33618618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104022822-A-C

http://identifiers.org/hco/11/GRCh38#33618621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104022819-C-A

33618621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 104022819-C-T

33618668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104022772-T-C

33618677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104022763-G-A

33618677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104022763-G-T

33618692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104022747-A-G

33618759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104022698-G-T

http://identifiers.org/hco/11/GRCh38#33618775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104022676-C-A

33618775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104022676-C-T

33619110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104022374-C-T

33619208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104022281-G-A

33619512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104021886-C-T

33619555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104021853-A-G

33620241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104020612-T-A

33620691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104019666-A-G

33620800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104019563-A-G

33621188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104019187-C-T

http://identifiers.org/hco/11/GRCh38#33621228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#104019146-C-A

33621275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104017708-T-G

33621331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104017658-C-T

33621590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104016013-T-C

33621615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104015991-A-G

http://identifiers.org/hco/11/GRCh38#33621756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104015854-A-C

http://identifiers.org/hco/11/GRCh38#33621991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104014688-C-A

33622114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104014079-C-T

33622828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104012951-G-A

33622837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104012943-C-T

http://identifiers.org/hco/11/GRCh38#33622886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104012902-C-A

33622886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104012902-C-T

33622946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104012824-G-T

33623058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104012699-T-C

33623449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104012330-G-A

33623475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104012304-T-A

33623475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104012304-T-C

33623481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104012298-G-A

33623542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104012234-C-T

33623991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104011812-C-T

33624021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104011793-G-T

33624239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104011593-G-A

33624284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104011549-C-T

33624285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104011548-T-C

33624466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104011375-C-G

33624466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104011375-C-T

33630978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104011297-T-C

33631148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104011155-T-A

33631155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104011148-C-T

http://identifiers.org/hco/11/GRCh38#33631300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104010982-C-A

33631300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104010982-C-T

http://identifiers.org/hco/11/GRCh38#33631369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104010912-C-A

33631409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104010872-C-T

33631574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104010754-C-T

33631681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104010667-G-C

http://identifiers.org/hco/11/GRCh38#33631770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104010542-C-A

http://identifiers.org/hco/11/GRCh38#33631972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104010343-A-C

33632075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104010253-C-T

33632144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104010181-T-C

33632173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104010152-G-T

33632194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104010131-T-G

33632300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104010026-C-T

33632953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104008975-G-T

33633349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104008935-G-A

33633349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104008935-G-T

33633365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104008919-G-C

33633523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104008751-G-A

33633570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104008704-G-A

33633813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104008496-G-A

33633813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104008496-G-C

33633813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104008496-G-T

33633983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104008318-G-A

33634448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104008131-G-A

33634588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104008015-G-C

33634645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104007964-T-C

33634720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 104007897-A-G

http://identifiers.org/hco/11/GRCh38#33634914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104007766-A-C

33634928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104007752-T-C

33634981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104007734-A-G

33635032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104007689-A-G

33635213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104007522-A-G

33635326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104007411-T-A

33635438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104007319-C-T

33635488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104007274-G-A

33635603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104007174-G-A

33635603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104007174-G-C

http://identifiers.org/hco/11/GRCh38#33635615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104007165-A-C

33635755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104007071-T-C

33635798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104007017-G-T

33635800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104007015-G-A

33637158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104006775-A-G

33637173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104006760-A-G

33637214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104006720-G-T

33637312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104006625-G-T

33637545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104006427-G-T

http://identifiers.org/hco/11/GRCh38#33637788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104006204-C-A

33638003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005981-C-T

33638124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005857-T-C

33638342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005658-G-T

http://identifiers.org/hco/11/GRCh38#33638354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104005647-A-C

33638354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005647-A-G

33638355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005646-T-A

33638355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005646-T-G

33638366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005638-G-A

33638366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005638-G-T

33638371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005633-T-A

33638371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005633-T-C

http://identifiers.org/hco/11/GRCh38#33638381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104005623-C-A

33638381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005623-C-G

33638381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005623-C-T

33638391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005614-T-C

33638499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005573-G-A

33638499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005573-G-C

33638499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005573-G-T

http://identifiers.org/hco/11/GRCh38#33638526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104005548-C-A

33638526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005548-C-T

33638552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005522-T-G

33638573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005501-A-T

33638585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005489-G-A

33638695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005393-T-C

33638747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005336-C-T

33638748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005335-C-T

33638947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005152-C-T

33638990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005118-T-C

33638996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104005112-C-G

33640060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104004091-G-T

33640132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104003895-A-G

33640399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104003219-A-T

33640639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104002995-C-T

33641152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104002481-G-A

33641191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104002439-C-T

33641193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104002437-A-G

33641211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104002419-C-T

33641301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104002335-G-A

33641476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104002210-G-A

http://identifiers.org/hco/11/GRCh38#33641553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104002136-A-C

33641553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104002136-A-G

33641553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104002136-A-T

33641755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104002043-A-T

33641792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104002002-C-T

33642015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104001812-A-G

33642025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104001802-C-T

33643367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104001435-G-A

33643625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104001179-A-G

33644051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104000574-T-C

http://identifiers.org/hco/11/GRCh38#33644086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104000545-A-C

33644327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 104000300-A-G

33644513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103999570-T-A

33644638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103999440-G-A

33644704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103999383-A-G

33644714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103999373-T-G

33644739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103999352-G-A

33645000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103999120-C-T

33645262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998888-A-G

http://identifiers.org/hco/11/GRCh38#33645477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103998706-C-A

33645477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998706-C-T

33645483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998700-G-A

33645483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998700-G-C

33645532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998666-T-C

http://identifiers.org/hco/11/GRCh38#33645533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103998665-A-C

33645561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998637-G-T

http://identifiers.org/hco/11/GRCh38#33645571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103998627-A-C

33645571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998627-A-T

33645608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998589-A-G

33645622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998575-A-G

33645625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998574-T-C

http://identifiers.org/hco/11/GRCh38#33645681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103998536-C-A

33645681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 103998536-C-T

33645713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 103998504-A-G

33645744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 103998473-A-G

33645773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 103998444-T-G

33645809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 103998408-G-A

33645863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 103998354-T-A

33645968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 103998249-C-T

33645971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 103998246-A-G

33645977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 103998240-G-A

33645977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: 103998240-G-T

http://identifiers.org/hco/11/GRCh38#33646004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103998213-C-A

33646042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998175-T-A

33646042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998175-T-C

http://identifiers.org/hco/11/GRCh38#33646063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103998154-C-A

33646063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998154-C-T

http://identifiers.org/hco/11/GRCh38#33646066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103998151-C-A

33646066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998151-C-G

33646066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998151-C-T

33646112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998104-G-A

33646137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103998096-G-T

33646294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103997988-C-T

33646393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103997889-A-G

33646393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103997889-A-T

33646413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103997869-G-A

33646429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103997854-G-A

33647676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103995896-T-G

33647678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103995894-G-A

33647709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103995864-T-G

33648437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103995496-A-T

33648474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103995460-C-G

33648508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103995425-G-T

33648576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103995349-T-A

33648652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103995282-G-T

33648826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103995113-G-T

33648842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103995097-C-T

http://identifiers.org/hco/11/GRCh38#33649049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103994894-A-C

33649673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103994277-C-G

33649701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103994273-A-G

33651961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103991819-T-C

33652025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103991756-C-T

33652033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103991748-C-T

33652198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103990486-G-A

33652299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103990374-G-A

33652299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103990374-G-T

33652328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103990357-C-T

33652334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103990351-A-G

33652444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103990247-C-T

33652445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103990246-T-C

33652451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103990238-C-T

33652827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103989904-T-C

33654257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron variant
orthologous variants: 103988923-C-T

33654692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103988538-C-G

33654692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103988538-C-T

33654866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103988352-G-A

33655118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103988124-T-C

33655192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103988060-C-T

33655232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103988023-G-A

33655239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103988015-A-G

33655281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 103987980-C-T

33655481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103987784-C-T

33655643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103987612-A-G

33655675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103987585-G-T

33655691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103987569-G-T

http://identifiers.org/hco/11/GRCh38#33655905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103987325-A-C

33655905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103987325-A-G

33655905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103987325-A-T

33656036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 103987199-G-C

http://identifiers.org/hco/11/GRCh38#33656057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103987178-C-A

http://identifiers.org/hco/11/GRCh38#33656162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103987049-C-A

33656193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103987024-A-G

33656564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103986662-A-G

33656889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103986302-C-T

33657045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103986160-C-T

33657366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103985868-C-T

33657390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103985845-T-A

33657390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103985845-T-C

33658420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985722-C-T

33658565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985589-G-A

33658565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985589-G-T

33658622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985535-A-G

33658622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985535-A-T

http://identifiers.org/hco/11/GRCh38#33658692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103985462-C-A

33658693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985461-T-A

33658693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985461-T-C

33658736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985415-T-A

33658736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985415-T-C

33658738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985413-T-A

33658738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985413-T-C

33658880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 103985271-T-C

33658880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 103985271-T-G

33658950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985217-G-A

33658950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985217-G-C

33658950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985217-G-T

http://identifiers.org/hco/11/GRCh38#33659016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103985169-C-A

33659016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985169-C-T

33659023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103985162-G-T

33659237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103984803-T-C

33659279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103984759-G-A

33659279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103984759-G-T

33659403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103984634-T-G

33659473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103984566-A-G

33659473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103984566-A-T

33659741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103984265-A-G

33659757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103984252-G-C

33659906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103984093-G-A

33659934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103984069-G-A

33660690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103983605-A-G

33660712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103983578-A-G

33660996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 103983293-G-A

33660996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 103983293-G-C

33660996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 103983293-G-T

http://identifiers.org/hco/11/GRCh38#33661091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103983198-A-C

33661096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103983194-G-A

http://identifiers.org/hco/11/GRCh38#33661110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103983180-C-A

33661110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103983180-C-T

33661114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103983176-G-T

http://identifiers.org/hco/11/GRCh38#33661274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103983023-A-C

33661303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103982987-C-G

33661365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103982918-G-A

33661498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103982789-T-A

33661515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103982770-T-A

http://identifiers.org/hco/11/GRCh38#33661517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103982768-A-C

33661582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103982704-T-C

33661582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103982704-T-G

33663460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103981896-C-T

33663634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103981753-T-C

33663657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103981748-C-G

33663917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103981504-G-A

33664003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103981422-G-A

33664049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103981376-A-G

33664535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103980952-G-C

33664535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103980952-G-T

33664607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103980875-T-G

33664796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103980725-A-T

33666543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103980205-A-T

33666571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103980177-T-C

33666616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103980129-G-A

33666954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103979780-T-C

33667828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, undefined
orthologous variants: 103979447-T-C

33667867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 103979411-C-G

33667996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 103979282-G-A

33668029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 103979249-G-T

33668239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103979036-A-G

33668250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103979025-G-T

http://identifiers.org/hco/11/GRCh38#33668263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103979011-C-A

http://identifiers.org/hco/11/GRCh38#33668267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103979007-C-A

33668267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103979007-C-T

http://identifiers.org/hco/11/GRCh38#33668290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103978986-A-C

33668290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103978986-A-G

33668397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103978877-T-C

33668429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103978843-A-G

33668442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103978830-C-T

33668560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103978717-G-A

33668622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103978654-C-G

33668622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103978654-C-T

33668651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103978610-G-T

33668672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103978587-A-G

33669096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103978173-A-G

33669427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103977884-A-G

33669433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103977878-G-A

33669466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103977850-A-T

33669561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 103977753-C-T

http://identifiers.org/hco/11/GRCh38#33670088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103977243-C-A

33670088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103977243-C-T

33670365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103976990-T-C

33670365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103976990-T-G

33670450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103976906-T-C

33670481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103976880-A-G

33670681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103976708-G-T

http://identifiers.org/hco/11/GRCh38#33670745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103976635-C-A

http://identifiers.org/hco/11/GRCh38#33670860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103976528-C-A

http://identifiers.org/hco/11/GRCh38#33670889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103976473-C-A

33670889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103976473-C-T

33670891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103976470-G-A

33670891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103976470-G-T

http://identifiers.org/hco/11/GRCh38#33670901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103976460-C-A

33670910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103976451-C-T

http://identifiers.org/hco/11/GRCh38#33670935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103976426-C-A

33670937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 103976424-T-C

33670976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 103976385-G-T

http://identifiers.org/hco/11/GRCh38#33670984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103976377-A-C

33671221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103976223-G-A

33671221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103976223-G-C

33671221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103976223-G-T

33671615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975836-C-T

33671637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975817-G-A

http://identifiers.org/hco/11/GRCh38#33671824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103975631-C-A

33671916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975558-A-G

http://identifiers.org/hco/11/GRCh38#33672054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103975476-C-A

33672054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975476-C-T

http://identifiers.org/hco/11/GRCh38#33672064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103975466-C-A

33672093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975442-A-G

http://identifiers.org/hco/11/GRCh38#33672181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103975375-C-A

33672181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975375-C-T

http://identifiers.org/hco/11/GRCh38#33672191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103975365-C-A

33672192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975364-T-C

33672236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975283-G-A

33672243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975276-C-T

http://identifiers.org/hco/11/GRCh38#33672290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103975233-C-A

33672290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975233-C-T

33672307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975219-T-C

33672336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975190-T-C

33672398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975123-A-G

33672402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975119-A-G

33672409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975112-G-A

33672409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975112-G-T

33672516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103975006-A-G

33672536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103974987-G-A

33672536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103974987-G-T

33672537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103974986-T-A

33672544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103974979-G-T

http://identifiers.org/hco/11/GRCh38#33672563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103974960-C-A

http://identifiers.org/hco/11/GRCh38#33672619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103974906-C-A

33672620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103974905-T-C

http://identifiers.org/hco/11/GRCh38#33672696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103974826-C-A

33672696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103974826-C-T

33672922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103974601-A-G

33672955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103974567-T-C

33673014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103974512-A-G

http://identifiers.org/hco/11/GRCh38#33673074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103974453-C-A

33673076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103974451-G-A

33673233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103974293-G-T

33673364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103974148-G-A

33673562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103973943-A-G

http://identifiers.org/hco/11/GRCh38#33673567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103973938-C-A

33673567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103973938-C-T

33673780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103973738-T-C

http://identifiers.org/hco/11/GRCh38#33673795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103973723-C-A

33673805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103973713-T-C

33673856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103973662-A-G

http://identifiers.org/hco/11/GRCh38#33673872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103973650-A-C

http://identifiers.org/hco/11/GRCh38#33673873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103973649-C-A

33673947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103973574-A-G

33673954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103973567-A-G

33673954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103973567-A-T

33674027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103973494-C-T

33674085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24836
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 103973435-G-A