115623787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42160760-G-A

http://identifiers.org/hco/3/GRCh38#115623792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42160750-C-A

115623892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42160640-T-C

115624306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42160237-T-G

115624366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42160177-A-G

http://identifiers.org/hco/3/GRCh38#115624370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42160173-A-C

115624721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42159807-G-A

115624721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42159807-G-C

115624765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42159778-G-A

115624873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42159666-T-G

115624905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42159632-G-A

115624910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42159628-T-G

115625115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42159421-G-A

115625297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42159249-G-T

115625387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42159170-C-G

115625387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42159170-C-T

115625483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42159072-G-C

115625932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42158613-G-A

115626301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42158244-C-T

http://identifiers.org/hco/3/GRCh38#115626769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42157798-A-C

115626777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42157791-C-T

115627091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42157484-A-T

115627260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42157349-C-G

115627283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42157325-T-C

115627753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42156846-G-A

115628006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42156581-G-T

115628563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42156115-A-G

115628586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42156094-C-G

115628783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42155931-T-G

115629175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42155594-C-T

115629250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42155520-G-T

115629283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42155485-C-T

115629297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42155471-T-C

115629964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42154853-C-T

115630160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42154638-A-G

115630204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42154614-T-A

115630382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42154434-G-A

115630523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42154282-A-G

115630554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42154262-G-A

115630554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42154262-G-T

115630662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42154159-G-T

115630737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42154086-C-T

115630929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42153862-G-A

115631036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42153761-G-A

115631179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42153626-T-A

http://identifiers.org/hco/3/GRCh38#115631180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42153625-C-A

115631516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42153331-A-G

115631947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42153215-G-A

115631994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42153168-G-T

115632234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42152860-C-T

115632285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42152809-G-A

http://identifiers.org/hco/3/GRCh38#115632360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42152741-A-C

115632421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42152686-A-T

http://identifiers.org/hco/3/GRCh38#115632430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42152677-C-A

115632456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42152651-A-G

115632488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42152615-G-A

115633060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42152066-A-G

115633240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42151869-G-A

115633406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42151733-G-C

115633503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42151560-G-T

115633507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42151556-G-A

115633671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42151157-G-A

115633671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42151157-G-C

115633671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42151157-G-T

115633963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42150882-T-C

115634039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42150779-T-C

115634150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42150669-G-A

115634212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42150608-A-G

115634239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42150582-C-T

115634405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42150427-T-G

115634411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42150421-G-C

115634953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42150031-C-T

115634972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42150017-A-G

115635085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42149948-A-T

115635232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42149827-T-C

115635321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42149735-A-T

115635735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42149392-A-G

http://identifiers.org/hco/3/GRCh38#115637353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42148516-A-C

115637994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42147947-G-A

115638052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42147791-C-T

115638469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42147396-T-C

115638696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42147181-T-C

115638705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42147172-A-G

http://identifiers.org/hco/3/GRCh38#115638749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42147129-C-A

115639017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42146955-T-C

115639022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42146950-T-C

115639738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42146597-C-T

115639905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42146457-C-G

115640009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42146340-A-G

115640034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42146317-T-G

115640068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42146285-T-C

115640350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42146008-G-A

http://identifiers.org/hco/3/GRCh38#115640409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42145953-C-A

115640732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42145618-G-T

115640796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42145570-G-A

115641231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42145422-C-T

115641283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42145368-A-T

115642142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42144205-C-T

115642172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42144175-A-T

115642552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42143984-T-C

115642610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42143938-G-A

115642696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42143855-C-G

115642739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42143751-C-T

115642869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42143624-T-C

115643185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42143332-A-T

115643201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42143317-T-G

115643274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42143244-G-A

115643300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42143218-C-T

115643353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42143170-T-C

115643465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42143064-A-G

115643638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42142878-C-T

115643673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42142844-A-G

115643773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42142748-T-C

115643800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42142716-C-T

115643847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42142669-C-T

http://identifiers.org/hco/3/GRCh38#115643993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42142525-C-A

115644013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42142505-C-T

115644271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42142246-G-A

115644712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42141813-T-A

115645052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42141479-G-T

115645733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42140848-G-A

115646696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42140009-A-T

115646724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42139981-A-G

115646742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42139962-A-T

115647159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42139722-T-C

115647398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42139523-G-A

115647398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42139523-G-T

115647772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42136699-G-A

115647947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42136544-G-A

115647964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42136527-T-C

115648203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42136320-T-C

http://identifiers.org/hco/3/GRCh38#115648671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42134508-A-C

115648678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42134501-G-A

115648854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42134343-C-T

115648936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42134258-A-G

115648936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42134258-A-T

115649114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42134046-A-T

115649144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42134016-G-A

115649301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42133841-A-G

http://identifiers.org/hco/3/GRCh38#115649444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42133247-C-A

115649444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42133247-C-T

115649536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42133158-A-G

115649665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42133042-G-T

115649882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42133018-C-T

115649896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42133004-A-T

115650375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42132534-T-C

http://identifiers.org/hco/3/GRCh38#115650448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42132471-A-C

115650458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42132461-G-A

115650489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42132430-G-C

115650494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42132425-C-T

115652749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42132126-C-T

http://identifiers.org/hco/3/GRCh38#115652839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42132035-C-A

115652839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42132035-C-T

115652947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42131933-C-T

115653121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42131772-T-A

115653499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42131702-A-G

115653556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42131663-A-G

115653577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42131642-G-A

115653641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42131579-A-G

115654429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42130761-T-C

http://identifiers.org/hco/3/GRCh38#115654743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42130461-A-C

115654743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42130461-A-T

115655082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42130101-G-A

115655242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42129941-G-A

115655417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42129772-A-G

115655827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42129355-A-G

115655891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42129289-C-G

115656424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42128780-T-A

115656514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42128689-T-C

115656522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42128681-G-A

http://identifiers.org/hco/3/GRCh38#115656975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42128032-C-A

115656975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42128032-C-T

115657053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42127924-A-G

115657087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42127890-G-C

115657375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42127607-T-A

115658287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42126988-T-G

http://identifiers.org/hco/3/GRCh38#115658383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42126920-A-C

http://identifiers.org/hco/3/GRCh38#115658407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42126885-C-A

115658407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42126885-C-T

115658416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42126876-C-T

http://identifiers.org/hco/3/GRCh38#115658426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42126866-C-A

115658426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42126866-C-T

115658505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42126729-T-C

http://identifiers.org/hco/3/GRCh38#115658506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42126728-C-A

115658509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42126725-T-C

115658534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126678-G-A

115658534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126678-G-T

http://identifiers.org/hco/3/GRCh38#115658548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#42126664-C-A

115658548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126664-C-T

115658555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126657-G-T

115658560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126652-C-T

http://identifiers.org/hco/3/GRCh38#115658714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#42126497-C-A

115658714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126497-C-T

115658795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126442-T-C

http://identifiers.org/hco/3/GRCh38#115658808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#42126429-C-A

http://identifiers.org/hco/3/GRCh38#115658851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#42126393-C-A

115658867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126377-G-T

115658921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126353-G-A

115658921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126353-G-T

115658990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126290-A-G

115658990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126290-A-T

http://identifiers.org/hco/3/GRCh38#115659037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#42126245-C-A

115659038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126244-T-A

115659038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126244-T-C

115659069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126213-T-C

115659212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126077-G-A

115659263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126031-A-G

115659292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42126002-A-G

115659302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42125992-C-T

115659734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42125606-T-C

115660015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42125319-C-T

115660170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42125146-C-T

115660399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42124896-T-C

115660425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42124866-A-G

115660662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42124492-G-C

115660805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42124360-T-A

115660828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42124344-G-A

115661190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42123997-G-T

115661303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42123880-T-C

115661304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42123879-G-T

115661327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42123863-G-T

115661329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42123861-C-G

115661944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42122738-A-T

115661981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42122697-A-T

115662002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42122681-G-A

115662002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42122681-G-C

115662002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42122681-G-T

115662018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42122668-G-A

115662033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42122653-A-G

115662201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42122478-A-G

115662307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42122370-G-T

115662469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42122249-G-A

115662581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42122166-G-A

115662656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42122084-C-T

115662820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42121758-A-G

115662854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42121719-A-G

115662898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42121676-A-G

115662929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42121649-G-A

115663155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42121417-T-C

115663430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42121189-T-A

115663430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42121189-T-G

115663431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42121188-A-G

http://identifiers.org/hco/3/GRCh38#115663478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42121137-A-C

115663478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42121137-A-G

115663494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42121121-T-C

115663494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42121121-T-G

115663507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42121107-T-C

115663600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42121013-A-T

115663616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42120997-A-G

115663668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42120944-C-G

115663675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42120934-T-C

115663869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, stop_gained
orthologous variants: 42120742-C-T

115663879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, missense_variant
orthologous variants: 42120732-C-G

115663899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, missense_variant
orthologous variants: 42120715-A-G

115664129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42120494-T-A

115664129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42120494-T-C

115664145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42120466-A-G

115664147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42120464-C-G

115664296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42120335-G-C

115664329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42120301-C-T

115665632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42120063-T-G

115665681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42120001-A-G

115665707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42119977-T-C

115666144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42119607-A-G

115666429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42119332-G-A

115666597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42118991-C-T

115666624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42118967-G-A

115666659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42118943-G-A

115666727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42118876-A-G

115666790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42118791-A-G

115666885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42118699-G-A

115666991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42118593-G-A

115667072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42118539-C-T

115667135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42118477-T-C

115667148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42118462-A-G

115668146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42117776-T-C

115668250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42117676-G-A

115670480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42117245-G-A

115670552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42117181-G-A

115670649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42117087-G-T

115671028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42116026-T-C

115671051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42116003-T-C

115671117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42115937-T-C

115673671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42115032-T-A

115673725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42114978-A-G

115673905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42114780-G-A

115673932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42114753-T-C

115674203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42114315-T-G

115674308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42114035-G-T

115674553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42113755-T-C

115674595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42113714-G-A

115675003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42113316-A-G

115675630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42112958-A-T

http://identifiers.org/hco/3/GRCh38#115676446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42112321-A-C

http://identifiers.org/hco/3/GRCh38#115676523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42112244-A-C

115676523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: missense variant
orthologous variants: 42112244-A-T

115676636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42112134-A-G

115676662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42112109-T-C

115676686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42112085-G-A

115676686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42112085-G-C

115676686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42112085-G-T

http://identifiers.org/hco/3/GRCh38#115676716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42112059-A-C

115677546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42111225-T-C

115677783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42110353-T-G

115678138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42110026-T-G

115678184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42109981-A-T

115678186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42109979-G-A

115678327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42109858-T-C

115678457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42109664-G-A

115678600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42109490-A-G

115678678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42109411-T-C

115678767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42109322-A-G

115679001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42108997-C-G

115679002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42108996-A-G

115679015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42108983-C-T

115679082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42108913-G-A

115679292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42108737-A-G

115679394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42108657-T-C

115679413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42108639-T-A

115679486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42108571-C-G

115679543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42108506-G-A

115679766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42108279-A-T

115679776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42108270-C-T

115679799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42108200-G-A

115680532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42107739-G-A

http://identifiers.org/hco/3/GRCh38#115680611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42107660-C-A

115680647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42107631-A-T

115680894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42107418-T-G

115680979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42107356-C-T

http://identifiers.org/hco/3/GRCh38#115681266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42107074-A-C

115681393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42106952-T-C

115681784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42106703-G-A

115681824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42106667-A-G

115681969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42106528-C-G

http://identifiers.org/hco/3/GRCh38#115681997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42106501-C-A

115682055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42106449-C-T

115682185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42106326-T-C

115682235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42106278-A-G

http://identifiers.org/hco/3/GRCh38#115682293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42106224-C-A

115684892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42105283-T-G

115685142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42104759-T-G

115685183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42104718-C-T

115685305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42104607-G-T

115685336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42104576-T-C

115685494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42104420-T-C

115685706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42104192-A-T

115685830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42104068-C-T

115686345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42102817-G-A

115686865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42102383-C-T

http://identifiers.org/hco/3/GRCh38#115687036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42102250-A-C

115687036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42102250-A-G

115687090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42102201-C-T

115687133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42102168-C-T

115687154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42102147-A-T

115687161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42102140-C-T

115687259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42102048-G-A

115687259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42102048-G-T

115687376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42101948-A-G

115687541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42101825-T-C

115687575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42101783-G-T

115687723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42101631-T-C

http://identifiers.org/hco/3/GRCh38#115687910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42101450-C-A

115688444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42100747-G-A

115688463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42100734-T-A

115688463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42100734-T-C

115688464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42100733-C-G

115688643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42100534-G-A

115688767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42100254-C-T

115689040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42099897-G-A

115689060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42099878-G-A

115689075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42099866-C-T

115689337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42099592-C-T

http://identifiers.org/hco/3/GRCh38#115689390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42099551-A-C

115689425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42099516-T-C

115689437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42099504-A-G

115689465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42099476-A-G

115690228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42099189-C-T

115690437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42098984-C-T

115690469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42098947-A-T

115690483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42098922-C-T

115691230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42098830-A-G

115691451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42098612-G-A

http://identifiers.org/hco/3/GRCh38#115691452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42098611-C-A

115691560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42098512-G-A

http://identifiers.org/hco/3/GRCh38#115692005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42098069-C-A

115692355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42097753-G-A

115692459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42097647-T-C

http://identifiers.org/hco/3/GRCh38#115692600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42097493-A-C

115692601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42097492-G-A

115692620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42097473-G-C

115692664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42097450-A-G

115692760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42097357-G-C

http://identifiers.org/hco/3/GRCh38#115693035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#42097048-C-A

115693059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42097037-C-T

115693986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42096161-G-T

115694081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42096065-G-A

115694185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42095958-C-G

http://identifiers.org/hco/3/GRCh38#115694402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42095738-A-C

115694547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42095395-A-G

115694619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42095330-A-T

115695024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42094959-G-T

http://identifiers.org/hco/3/GRCh38#115695115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42094885-C-A

115695343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42094673-G-A

115695527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42094529-G-A

http://identifiers.org/hco/3/GRCh38#115697573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42092344-C-A

115697605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42092310-T-C

115697668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42091883-A-G

http://identifiers.org/hco/3/GRCh38#115697889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42091664-C-A

115697950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42091621-G-A

115697979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42091592-A-G

http://identifiers.org/hco/3/GRCh38#115697984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42091587-C-A

115697984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42091587-C-T

http://identifiers.org/hco/3/GRCh38#115698014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42091556-A-C

115698063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42091508-A-T

115698067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42091504-T-A

115698067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42091504-T-C

115698239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42091135-A-T

115698278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42091096-T-A

115698278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42091096-T-G

115698296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42091079-A-T

115698535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42090730-C-G

115698568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42090708-G-C

115698622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42090654-G-C

115698726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42090556-G-A

http://identifiers.org/hco/3/GRCh38#115698788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42090493-C-A

115698929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42090356-T-C

115699056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42090212-A-G

115699075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42090192-T-A

115699091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42090176-C-T

115699213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42090057-G-A

115699213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42090057-G-C

115699333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42089940-C-T

115699545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42089727-C-T

115699871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42089392-G-T

115700410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42088929-C-G

115701110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42087564-T-C

115701220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42087494-T-G

115701223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42087491-A-G

http://identifiers.org/hco/3/GRCh38#115701390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42087341-A-C

115701500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42087242-G-C

115701737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42087009-T-C

115701893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42086880-A-G

115701901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42086872-A-G

115701943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42086838-C-T

115702052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42086748-G-A

115702052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42086748-G-T

115702071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42086729-T-C

115702110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42086686-C-G

115702111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42086685-C-T

115702408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42086244-G-A

115702453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42086212-T-C

115703025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42085669-C-T

115703105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42085585-G-A

115703127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42085556-G-A

115703237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42085461-G-A

115703421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42085287-G-A

115703424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42085284-G-A

115703465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42085242-T-A

115703924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42084627-A-G

115704443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42084098-C-T

115704730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42083812-A-T

http://identifiers.org/hco/3/GRCh38#115704752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42083794-A-C

115704770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42083776-G-T

115705700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42082363-T-G

115705822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42082192-A-G

115705872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42082072-G-C

115705949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42081990-C-T

115706033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42081919-C-G

115706139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42081428-C-T

http://identifiers.org/hco/3/GRCh38#115706380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42081178-A-C

115706394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42081164-A-G

115706394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42081164-A-T

115706516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42081024-T-C

http://identifiers.org/hco/3/GRCh38#115706622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42080950-C-A

115707661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42079867-T-G

115707759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42079780-T-G

115708024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42079552-T-C

115708211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42079382-C-G

115711368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42078601-A-G

115711679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42078307-C-G

115711703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42078251-C-T

115711731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42078202-A-G

115711878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42078061-T-C

115712239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42077361-G-T

115712307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42077299-A-G

115712337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42077275-A-G

115712405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42077230-G-A

115713153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42076518-A-G

http://identifiers.org/hco/3/GRCh38#115713542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42076138-C-A

115713542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42076138-C-G

115713542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42076138-C-T

115713613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42076059-C-T

115713690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42075993-C-G

115713782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron_variant, undefined
orthologous variants: 42075894-A-G

115713796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42075880-T-C

115713798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42075878-G-C

115713987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42075562-C-T

115714265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42075266-A-G

115714471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42075065-G-A

115714491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42075050-A-G

115714592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42074944-A-G

115714754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42074828-G-T

115714898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42074717-T-C

115714898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42074717-T-G

115714948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42074651-G-A

115714948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42074651-G-T

115715019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42074513-A-G

115715178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42074350-G-C

115715392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42074130-T-G

115715709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42073799-T-C

115715759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42073751-G-T

115715800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42073710-G-A

115716015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42073487-A-G

115716689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42072819-A-G

115717018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42072539-T-G

http://identifiers.org/hco/3/GRCh38#115717175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42072390-A-C

115717187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42072379-G-A

115717216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42072338-A-G

115717235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42072320-G-A

115717235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42072320-G-C

115717913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42071992-G-T

115718093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42071811-C-T

115719880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42070631-G-A

115719920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42070588-T-G

115719952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42070549-T-C

115719956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42070545-C-T

115720393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: intron variant
orthologous variants: 42070067-A-G

http://identifiers.org/hco/3/GRCh38#115721020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#42069260-C-A

115721020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4140
most severe consequence: 3 prime UTR variant
orthologous variants: 42069260-C-T