97588598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68804469-C-T

97593806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798886-A-G

97593810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798882-G-T

97593816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798876-G-C

97593905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798790-T-C

97593923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798772-A-G

97593924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798771-C-T

97593950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68798745-G-A

97595033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68797883-T-C

http://identifiers.org/hco/15/GRCh38#97595806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68797207-C-A

http://identifiers.org/hco/15/GRCh38#97595975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68797061-C-A

97596136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796906-A-G

http://identifiers.org/hco/15/GRCh38#97596220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68796821-A-C

97596301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796760-G-T

http://identifiers.org/hco/15/GRCh38#97596355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68796706-A-C

97596876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796577-A-G

97596938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796521-G-C

97596938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796521-G-T

97596972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796487-C-T

97597027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796443-T-A

97597027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796443-T-C

97597192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796303-C-T

97597272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796222-A-G

http://identifiers.org/hco/15/GRCh38#97597294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68796200-A-C

97597303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796188-G-A

97597403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68796047-A-G

97597471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795980-T-G

97597475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795976-T-C

97597490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795961-A-T

97597754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795733-G-C

97597840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795654-C-T

97597842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795652-T-C

97598178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795384-T-C

97598249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795326-G-A

http://identifiers.org/hco/15/GRCh38#97598260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68795315-C-A

97598260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795315-C-T

97598338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68795247-C-T

97598988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68794599-G-A

97599094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68794491-G-A

97599462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68793849-C-G

97599463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68793848-T-C

97599631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68793675-T-C

97599664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68793643-G-A

97601418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68792717-G-A

97601471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68792665-T-G

97601988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68792214-T-C

97602223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68792036-C-T

97602357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68791907-T-C

97602465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68791797-A-T

97602935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68791358-T-C

97603825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68790486-A-T

97603993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68790322-G-A

97604247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68790105-T-C

97604357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68790014-T-A

97604410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789966-T-A

97604410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789966-T-G

97604421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789955-C-T

97604649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789755-T-G

97604709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789710-G-A

97604709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789710-G-C

97604709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789710-G-T

http://identifiers.org/hco/15/GRCh38#97604712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68789707-A-C

97604712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789707-A-G

97604715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789704-T-A

97604715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789704-T-C

97604734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789682-T-A

97604868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789558-G-A

97605133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789317-G-A

97605348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68789174-T-C

97606039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788491-A-G

97606051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788461-G-T

97606069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788440-C-T

97606070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788439-G-A

97606097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788415-C-G

97606097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788415-C-T

97606107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788403-G-A

97606124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788381-G-T

97606504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788036-A-G

97606505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68788035-T-C

97606558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787977-G-A

97606896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787655-T-C

http://identifiers.org/hco/15/GRCh38#97606911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68787640-A-C

97606937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787614-G-C

http://identifiers.org/hco/15/GRCh38#97606968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68787583-A-C

97606968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787583-A-G

97606976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787575-C-T

97607006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787564-T-A

97607347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787244-C-T

97607454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787148-G-A

97607454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68787148-G-C

97617241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68783986-A-G

97617450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68783791-A-G

97618575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68783015-G-T

97618673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68782829-T-G

97618864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68782611-T-C

http://identifiers.org/hco/15/GRCh38#97618887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68782595-C-A

97620426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68779819-T-A

97620761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68779481-C-G

97620761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68779481-C-T

97620855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68779399-C-T

97620944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68779318-T-A

97620951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68779311-G-A

97621171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68779155-T-A

97621445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68778902-A-T

97621947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68778390-C-T

97622141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68778221-T-A

97622152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68778210-A-G

97622318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68778037-A-G

97622461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68777886-T-A

97622499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68777848-T-C

97622710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68777638-T-A

97622791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68777557-C-G

97622791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68777557-C-T

97623267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68777067-A-T

97623290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68777048-G-A

97623391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68776947-G-A

97623430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68776907-C-T

97624042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68776304-G-A

97624076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68776272-C-G

97624157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68776184-T-A

http://identifiers.org/hco/15/GRCh38#97624473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68775900-A-C

97624603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68775773-C-G

97624697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68773326-C-G

http://identifiers.org/hco/15/GRCh38#97624839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68773188-C-A

97624914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68773106-C-T

97624999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68773046-C-T

97625010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68773034-T-C

97625028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68773015-G-A

97625028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68773015-G-T

97625065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68772979-A-T

97625188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68772848-T-A

97625231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68772808-T-C

http://identifiers.org/hco/15/GRCh38#97625249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68772747-C-A

97625336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68772671-C-T

97625467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68772560-G-T

97625621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68772439-T-C

97625630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68772434-G-A

97625653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68772411-T-C

http://identifiers.org/hco/15/GRCh38#97626798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68772030-C-A

http://identifiers.org/hco/15/GRCh38#97626808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68772018-A-C

97626872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68771963-G-C

97626987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68771858-A-G

97627135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68770373-G-C

97627166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68770342-C-T

97627401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68770121-G-A

97627533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68770012-T-C

97627598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68769945-G-A

97627709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68769821-T-C

97627746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68769784-C-T

97627890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68769664-C-T

97627898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68769656-C-T

97627950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68769591-C-T

97627994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68769545-A-G

97627994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68769545-A-T

97628187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68769196-T-C

http://identifiers.org/hco/15/GRCh38#97628221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68769162-A-C

97628500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68768898-T-A

97628500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68768898-T-C

97628568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68768824-G-A

http://identifiers.org/hco/15/GRCh38#97631193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68768613-C-A

97631323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68768497-T-A

97631323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68768497-T-C

97631340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68768480-T-C

97631340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68768480-T-G

97631357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68768463-A-G

97637172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68764822-C-T

97637303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68764691-G-C

97637303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68764691-G-T

97637488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68764496-C-G

97637588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68764399-T-A

97639725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68762463-C-T

97639726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68762462-A-G

97640189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68762042-T-C

97640209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68762022-A-G

97640225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68762006-T-A

97640309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68761921-T-G

97640528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68761702-A-G

97649839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68753638-G-A

97649844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68753633-T-C

97649875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68753600-G-A

97650421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68750751-G-A

97650507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68750666-C-G

97650507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68750666-C-T

97650588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68750596-A-G

97650625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68750557-G-A

97651978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68750052-A-T

97651984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68750046-A-G

http://identifiers.org/hco/15/GRCh38#97652162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68749876-A-C

97652522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68749524-T-C

97652701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68749358-G-T

97652713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68749348-G-C

http://identifiers.org/hco/15/GRCh38#97652743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68749327-A-C

97652867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68749212-G-A

97653049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 68749043-C-G

97653076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68749014-G-A

97653076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68749014-G-T

97653139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68748956-G-T

97653154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68748944-A-G

97653161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68748937-G-A

97653161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68748937-G-T

97653178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68748920-T-C

97653178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68748920-T-G

97653179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68748919-T-C

97653216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68748877-A-G

97653234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68748860-G-T

97653335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68748759-A-T

97653363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68748718-G-C

97653366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68748715-A-G

97653824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68748292-A-T

97653887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68748226-C-T

97653893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68748220-G-A

97654042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68748091-T-C

97654094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68748038-G-A

97654167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68747967-G-A

97654219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68747906-T-G

97654329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68747798-T-A

97654329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68747798-T-C

97655541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746515-T-C

97655556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746500-G-A

97655556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746500-G-T

97655906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746284-C-T

97655960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746230-T-C

97656025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68746171-A-G

97656212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68745948-T-G

97656284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68745877-A-G

97656304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68745857-C-T

97656573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68745598-G-A

97656573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68745598-G-T

97657174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68744532-G-A

97657723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68743998-A-G

http://identifiers.org/hco/15/GRCh38#97658113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68743649-C-A

http://identifiers.org/hco/15/GRCh38#97658182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68743599-A-C

97659201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68741816-G-A

http://identifiers.org/hco/15/GRCh38#97660156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68739004-C-A

97660531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68738649-T-C

97664339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68733789-A-T

97664493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68733644-T-C

97664582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68733561-T-C

97664590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68733553-C-T

97664705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68733431-T-G

97664753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68733398-T-C

97665280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68732882-G-C

97665342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68732824-T-A

97665342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68732824-T-C

97665398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68732769-T-C

97665525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68732653-T-A

97665828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68731836-A-G

97665828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68731836-A-T

97665843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68731821-T-C

97665859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68731805-C-T

http://identifiers.org/hco/15/GRCh38#97665991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68731676-A-C

http://identifiers.org/hco/15/GRCh38#97666066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68731608-A-C

97666159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68731482-T-C

97666245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68731425-T-C

97666383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68731273-C-T

97666415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68731244-G-T

http://identifiers.org/hco/15/GRCh38#97666491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68731199-A-C

97666791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68730864-A-G

97666886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68730763-T-C

97667245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68730452-G-A

97667515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68730195-T-G

97667901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68729811-G-A

97667901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68729811-G-T

97684529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68725460-A-T

97684964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68725210-C-T

97685170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68725036-T-G

97685362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68724851-A-G

97685392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68724821-A-G

97686711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68722707-C-G

97686739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68722678-G-A

97686747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68722670-A-G

http://identifiers.org/hco/15/GRCh38#97686871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68722516-C-A

97686871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68722516-C-G

97686871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68722516-C-T

97686872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68722515-G-A

http://identifiers.org/hco/15/GRCh38#97686954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68722433-C-A

97686963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68722424-C-T

97690515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68713832-T-C

http://identifiers.org/hco/15/GRCh38#97691196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68713550-C-A

http://identifiers.org/hco/15/GRCh38#97691235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68713513-C-A

97691235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68713513-C-G

97691235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68713513-C-T

97691244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 68713504-C-T

97691251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68713497-G-A

97691291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68713456-G-A

97691291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68713456-G-T

97691874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68713020-C-T

http://identifiers.org/hco/15/GRCh38#97691893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68713001-A-C

97692085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68712804-G-A

97692155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68712734-T-C

97692421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68712461-C-T

97693138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68711779-T-G

97693144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68711776-T-A

97693149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68711771-T-C

97693754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68711161-C-T

97693963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68710920-T-C

97694057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68710830-G-A

97694123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68710761-C-T

97694235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68710671-C-T

http://identifiers.org/hco/15/GRCh38#97694463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68710448-C-A

97694492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68710420-T-C

97694996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68709960-G-A

97695100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68709834-T-A

http://identifiers.org/hco/15/GRCh38#97695317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68709616-C-A

97695684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68709246-T-C

97699243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68707668-C-T

97699468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68707431-G-A

http://identifiers.org/hco/15/GRCh38#97699595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68707315-A-C

97699812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68707091-T-G

97700067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68706088-C-T

97700185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68705988-G-T

97700548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68705682-T-A

97700577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68705652-C-T

97700578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68705651-G-A

97701390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68702917-C-T

97701524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68702807-T-C

97701795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68702541-C-T

http://identifiers.org/hco/15/GRCh38#97701853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68702483-C-A

97702987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68701306-G-T

97703062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68701230-G-C

97703195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68701102-T-C

http://identifiers.org/hco/15/GRCh38#97705343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68698415-C-A

97705343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68698415-C-G

97705344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68698414-T-C

97705403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68698358-A-T

97705419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68698335-T-C

97705507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68698247-T-C

97705587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68698169-T-C

97705596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68698162-C-T

97705773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68697985-A-G

http://identifiers.org/hco/15/GRCh38#97705790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68697964-C-A

97705790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68697964-C-T

97705918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68697835-A-T

97706117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68697647-A-T

97706154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68697609-G-A

97706154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68697609-G-C

97706315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68697491-G-C

97706483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68697326-G-C

97706551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68697259-G-C

97706987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68697107-A-G

97707020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68697074-C-T

97707025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68697067-G-T

97707026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68697066-G-T

97707084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68697022-T-C

97707089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68697017-G-C

http://identifiers.org/hco/15/GRCh38#97707101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68697005-C-A

97707739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68693215-T-C

97707998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68692956-G-T

97708222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68692727-G-A

http://identifiers.org/hco/15/GRCh38#97708472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68692173-A-C

97708640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68691962-A-G

97708674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68691930-A-G

97708989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68691608-C-T

97709545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68691058-G-A

97709552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68691052-G-T

97709608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68691003-G-C

97709731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68689534-A-T

97709780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68689485-C-T

97709792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68689473-A-G

97709828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68689440-C-G

97710041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68689275-A-G

97710145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68689177-G-C

97710270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68689055-C-T

97710624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68688718-T-C

http://identifiers.org/hco/15/GRCh38#97710677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68688666-C-A

http://identifiers.org/hco/15/GRCh38#97710700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68688529-C-A

97710719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68688503-G-T

97710732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68688491-G-A

97710833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68688393-C-T

97710837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68688389-T-A

97710946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68688323-G-A

97710963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68688306-A-G

97711070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68688210-C-G

97712112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68686800-T-A

97712281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68686634-A-T

97712324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68686591-A-G

97712390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68686539-C-T

97712454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68686475-A-T

97712461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68686468-C-T

97713039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68685877-T-G

97713059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68685858-T-A

97713059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68685858-T-G

97713150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68685729-C-T

97713483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68685420-T-C

97713615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68685293-T-C

http://identifiers.org/hco/15/GRCh38#97713759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68685151-A-C

97713788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68685087-A-G

97713873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68684825-G-C

http://identifiers.org/hco/15/GRCh38#97713987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68684647-A-C

http://identifiers.org/hco/15/GRCh38#97713989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68684645-C-A

http://identifiers.org/hco/15/GRCh38#97713993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68684641-C-A

97714093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68684534-C-T

97714110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68684518-C-T

97715869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68683620-T-C

97716096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68683387-T-C

97717079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68682035-T-C

97717223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681873-G-T

97717373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681729-T-G

97717433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681671-C-T

97717694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681435-C-T

http://identifiers.org/hco/15/GRCh38#97717886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68681300-C-A

97717886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681300-C-T

97717937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681251-C-T

97717962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681226-A-T

97717995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681149-C-T

97718001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681143-G-A

http://identifiers.org/hco/15/GRCh38#97718002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68681142-C-A

97718051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681096-C-G

97718076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681071-C-T

97718148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68681020-G-A

97718200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68680969-T-A

97727452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68670716-T-A

97727654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68669624-C-T

97727721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68669561-T-C

97727722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68669560-C-T

97727763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68669520-T-C

http://identifiers.org/hco/15/GRCh38#97727783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68669500-A-C

97727795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68669488-C-T

97727828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68669456-T-C

97729400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68666182-G-A

97729495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68666103-G-A

97729565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68666033-T-A

97729620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68665981-G-A

97729639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68665963-G-A

97729639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68665963-G-C

97729681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68665934-C-T

97729771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68665846-C-G

97729771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68665846-C-T

97729787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68665830-T-G

97729978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68665336-A-G

97730034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68665242-C-T

97730278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68664988-C-T

97730565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68664670-G-A

97730858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68664510-T-C

97730983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68664376-A-T

97731311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68664052-C-T

97731397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68663969-T-C

97731421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68663948-T-C

http://identifiers.org/hco/15/GRCh38#97731492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68663881-A-C

97731503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68663870-G-A

http://identifiers.org/hco/15/GRCh38#97731537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68663842-C-A

97731693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68663703-C-T

http://identifiers.org/hco/15/GRCh38#97731700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68663696-A-C

97732943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68662603-T-A

97733063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68662482-A-G

97733096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68662463-T-C

http://identifiers.org/hco/15/GRCh38#97733259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68662314-A-C

97733297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68662280-C-T

97733330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68662247-T-C

97733860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68661730-T-A

97733861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68661729-T-C

97733862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68661728-T-C

97734088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68661510-G-A

97734102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68661495-G-A

97734102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68661495-G-T

97734328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68661313-T-C

97734358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68661286-G-T

97734441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68661126-C-G

97734837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68660699-T-C

97734949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68660586-T-C

97734969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68660569-G-A

97735094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68660431-A-G

97735240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68660095-T-C

http://identifiers.org/hco/15/GRCh38#97735290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68660034-C-A

97735290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68660034-C-T

97735463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68659894-T-C

http://identifiers.org/hco/15/GRCh38#97735780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68659571-A-C

http://identifiers.org/hco/15/GRCh38#97735886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68659461-A-C

97736140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68659218-A-T

97736670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68658662-G-A

97737036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68658297-T-A

97737063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68658268-T-A

97737078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68658253-T-C

97737343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68657988-A-G

97737442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68657770-G-A

97737783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68657369-G-A

97737940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68657235-T-C

http://identifiers.org/hco/15/GRCh38#97737965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68657210-A-C

97737965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68657210-A-T

97739118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68656559-G-T

97739373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68656322-C-T

97739475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68655005-C-G

97739913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68654578-G-T

97740699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68646990-G-A

97741004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68646694-G-A

97741088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68646608-G-A

97741226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68646472-C-T

97743948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68639426-C-G

97743948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68639426-C-T

97744029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68639356-C-G

97744029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68639356-C-T

97744194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68639196-T-A

97744543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68637720-C-G

97744721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68637575-T-G

97744750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68637546-A-G

97744820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68637468-T-G

97744845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68637440-T-A

97745111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68637180-A-T

http://identifiers.org/hco/15/GRCh38#97745310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68636937-C-A

97745310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68636937-C-G

97745697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68636598-G-C

97745839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68636435-A-G

97745982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68636300-T-G

97745985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68636297-G-T

97746027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68636261-C-G

97746662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68635490-T-C

97747104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68634992-G-A

97747396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68634771-G-A

97747458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68634709-A-G

97747931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68634297-G-A

97748187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68634048-G-A

97748187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68634048-G-T

97748358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68633879-G-C

97748797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68633436-G-A

97749394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632839-G-A

97749521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632726-C-G

97749521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632726-C-T

97749557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632690-C-T

97749613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632634-T-C

97749613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632634-T-G

97749689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632560-G-A

97749713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632539-T-G

97750088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68632166-A-G

http://identifiers.org/hco/15/GRCh38#97750202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68632050-C-A

97750268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68631984-T-C

97750313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68631939-G-C

97750388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68631864-G-C

97750843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68631369-C-T

97750862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68631350-G-T

97751272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630936-C-T

http://identifiers.org/hco/15/GRCh38#97751572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68630654-A-C

http://identifiers.org/hco/15/GRCh38#97751694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68630553-C-A

97751694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630553-C-T

97751708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630539-A-T

97751953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630273-T-C

97751974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630257-C-T

97751992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630246-A-G

97752200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68630053-A-G

97752315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68629944-A-G

97752329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68629930-G-A

97752344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68629915-C-T

97752370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68629889-A-T

97752524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68629734-T-C

http://identifiers.org/hco/15/GRCh38#97752532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68629726-C-A

97752667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68629593-G-A

97752788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68629472-A-G

97752850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68629406-A-G

97753029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68629216-T-C

97753330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68628865-T-C

97753489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68628701-T-G

97753542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68628658-T-G

97753748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68628556-T-G

97753752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68628552-A-G

97753972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68628329-C-T

97754021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68628303-A-G

97754454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68628011-T-A

97754454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68628011-T-C

97754828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627584-G-T

97755065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627310-T-A

97755287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68627077-C-G

http://identifiers.org/hco/15/GRCh38#97755338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68627026-A-C

97755401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68626963-T-G

97755605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68626770-T-C

97755605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68626770-T-G

97755655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68626717-T-A

97755657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68626715-T-A

http://identifiers.org/hco/15/GRCh38#97755866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68626535-C-A

97755866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68626535-C-G

97755866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68626535-C-T

97755898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68626500-C-T

97755993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68626419-T-C

97756766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68625903-C-T

97756937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68625762-C-T

97757115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68625575-G-T

97757161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68625494-G-T

http://identifiers.org/hco/15/GRCh38#97757215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68625357-C-A

97757284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68625276-A-G

http://identifiers.org/hco/15/GRCh38#97760516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68622491-A-C

97760634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68622363-G-C

97760851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68621516-A-T

97761055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68621331-T-G

97761153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68621175-G-A

97761250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68621079-G-A

97764786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68620042-T-C

97764812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68620016-C-T

97764863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68619968-G-T

97765346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68619553-G-C

97765510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68619416-T-A

97765546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68619385-T-C

97765586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68619344-C-T

97765711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68619234-G-A

97765775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68619171-T-A

97765956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68619004-T-C

97781683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68610096-C-G

97781756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68610021-G-T

97781788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609987-T-C

97781877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609896-G-A

97782054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609734-T-C

97782119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609676-G-A

97782119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609676-G-C

http://identifiers.org/hco/15/GRCh38#97782177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68609639-C-A

97782195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609621-G-A

97782195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609621-G-T

97782412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609406-T-C

97782467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609367-C-T

97782513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609326-C-T

97782693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68609118-C-G

97782879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608976-T-G

97783070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608765-G-A

97783181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68608657-C-T

http://identifiers.org/hco/15/GRCh38#97784119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68606912-A-C

http://identifiers.org/hco/15/GRCh38#97784141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68606889-A-C

http://identifiers.org/hco/15/GRCh38#97784144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68606886-A-C

97784196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606831-T-G

97784299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606741-A-T

97784318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606722-G-A

97784318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606722-G-T

97784337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68606703-G-A

97784840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68605739-T-C

97785056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68605516-T-C

http://identifiers.org/hco/15/GRCh38#97785069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68605503-C-A

97785069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68605503-C-T

97785542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68605336-A-G

97785569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68605302-T-C

97785648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68605217-G-A

97785834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68605035-C-T

97785850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68605019-G-T

97785865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68604999-T-C

97785928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68604938-G-A

http://identifiers.org/hco/15/GRCh38#97785974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68604894-C-A

http://identifiers.org/hco/15/GRCh38#97786012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68604856-A-C

97786673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603829-G-A

97786750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603752-T-G

97787054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603478-G-C

97787054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603478-G-T

97787058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603474-T-A

97787516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603353-T-C

97789044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68603061-G-A

http://identifiers.org/hco/15/GRCh38#97789086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68603026-C-A

97789317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68602801-G-T

97789601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68602525-G-A

97789635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68602460-C-T

97790951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68599146-A-G

http://identifiers.org/hco/15/GRCh38#97792248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#68595955-A-C

97792248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68595955-A-G

97792322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595881-G-C

97792416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68595790-C-T

97792505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595700-G-A

97792587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595618-G-A

97792857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595382-G-T

97793134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595134-C-T

97793139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595129-G-A

97793139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68595129-G-T

97793319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68594977-G-T

97793530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68594862-T-A

97793594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68594801-T-C

97793713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68594710-T-A

http://identifiers.org/hco/15/GRCh38#97793731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68594690-C-A

97793956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68594456-G-A

97794046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68594363-A-G

97794182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68594212-G-A

97794418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68593982-C-G

97794587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68593808-T-G

97794618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68593791-T-A

97794697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68593734-T-A

97794769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68593663-G-A

97794769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68593663-G-T

97795555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68592896-G-A

http://identifiers.org/hco/15/GRCh38#97795881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68592571-A-C

97796032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68592426-A-G

97796065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68592393-A-G

97796260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68592211-G-A

97796260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68592211-G-C

97796310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68592158-G-A

97796403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68592065-G-A

97796454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68592014-A-G

97796705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68591825-A-T

97796873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68591680-G-C

97796987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68591605-T-C

97797110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68591488-C-T

97797152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68591458-G-A

97797218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68591396-G-T

http://identifiers.org/hco/15/GRCh38#97797262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68591352-A-C

97797389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68590611-G-C

http://identifiers.org/hco/15/GRCh38#97797392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68590608-C-A

97797750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68589792-A-G

97797752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68589790-G-A

97797785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68589759-T-A

97797785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68589759-T-C

97797788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68589756-C-T

97797803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68589741-T-C

97797803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68589741-T-G

97798160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68589365-T-A

97798211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68589316-A-G

97798897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68588606-T-C

97798993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68588518-T-C

97799081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68588474-T-G

97799090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68588465-T-C

97799166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68588417-G-A

97799374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68588196-A-G

97799400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68588170-C-T

97799813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68586567-C-T

97799820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68586560-A-G

97800051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68586322-G-A

97800051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68586322-G-C

97800132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68586244-T-C

97800274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68586097-G-A

97800299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68586072-T-C

97800320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68586049-C-G

97800755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68585153-C-T

97800777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68585132-A-T

97800819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68585090-C-T

97800831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68585081-C-G

97800883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68585034-C-G

97801248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68584557-G-C

97801248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68584557-G-T

97801269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68584533-A-G

97801352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68584450-A-G

97801412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68584392-G-A

97801890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68581535-G-A

97801890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68581535-G-T

97802161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68581280-C-T

http://identifiers.org/hco/15/GRCh38#97802260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68581191-A-C

97802379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68581102-T-G

97802449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68581055-C-T

97802478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68581026-T-G

97802502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68580993-A-G

97802512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68580983-G-A

97802667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68580828-T-C

http://identifiers.org/hco/15/GRCh38#97803270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68580309-C-A

97803338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68580225-A-G

97803447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68580123-G-A

97803497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68580061-T-C

97803528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68580031-C-G

http://identifiers.org/hco/15/GRCh38#97803534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68580025-C-A

97803534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68580025-C-T

97803539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68580020-C-G

http://identifiers.org/hco/15/GRCh38#97803540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68580019-C-A

97803540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68580019-C-G

97803540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68580019-C-T

97803545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68580014-C-T

97804123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68578705-T-G

97804262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68578614-C-T

97804435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68578456-C-T

97804436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68578455-A-G

97804729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68578106-G-C

97804803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68578028-C-T

97805456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68577424-G-C

97805788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68576759-T-C

97806025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68576527-G-A

97806502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68575834-T-G

97806858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68575480-C-G

97807091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68575248-C-T

97807290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68575056-T-C

97807292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68575054-A-G

97807563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68574622-C-T

97807647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68574560-G-A

97807647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68574560-G-T

http://identifiers.org/hco/15/GRCh38#97807697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68574513-A-C

97807809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68574423-T-C

97807944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68574275-G-T

97807970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68574251-C-G

97807992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68574239-C-T

97808387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68573781-G-C

97808433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68573743-G-A

http://identifiers.org/hco/15/GRCh38#97808444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68573732-C-A

97808444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68573732-C-T

97808499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68573686-G-A

97808623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68573593-C-T

97808871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68573369-G-T

97808884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68573338-A-G

97808915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68573306-A-T

97808941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68573279-T-C

97809022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68573211-T-A

97809022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68573211-T-C

97809044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68573189-T-G

97809045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68573188-G-A

97809055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68573178-G-A

97809264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68572994-C-T

http://identifiers.org/hco/15/GRCh38#97809391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68572903-C-A

97809391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68572903-C-T

http://identifiers.org/hco/15/GRCh38#97809435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68572859-C-A

97809435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68572859-C-T

97809447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68572847-A-G

97809655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68572655-A-G

97813769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68571456-A-G

97814040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68571188-T-G

97814210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68571027-T-C

97814211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68571026-G-C

97814315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68570931-G-C

97814337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68570910-T-C

97814402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68570846-G-A

97814436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68570811-G-A

97814571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68570683-T-G

97814659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68570599-G-A

97814693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68570566-T-C

http://identifiers.org/hco/15/GRCh38#97814705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68570548-A-C

97814755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68570508-C-T

97814811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68570451-C-T

97815061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68570039-C-G

97815061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68570039-C-T

97815092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68569901-G-A

97815099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68569894-T-C

97815111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68569882-T-A

97815263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68569729-T-A

97815341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68569650-G-A

97815422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68569573-C-T

97815486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68569513-T-C

97815549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68569451-A-G

97815592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68569394-T-C

97816264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68568745-T-C

97816424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68568579-G-T

97816558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68568489-T-C

97816594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68568464-T-A

97816783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68568277-C-T

97816890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68568170-C-T

97816952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68568113-G-T

97816973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68568089-G-C

97817231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68567819-A-G

97817355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68567692-G-A

97817722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68567323-G-A

97817811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68567234-T-A

97817918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68567128-G-T

97818009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68567036-A-G

97818030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68567003-T-C

97818116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68566858-G-C

97818116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68566858-G-T

97818222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68566741-C-T

97818362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68566643-T-C

97818467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68566532-T-C

97818528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68566462-T-C

http://identifiers.org/hco/15/GRCh38#97818541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68566447-A-C

97818553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68566435-T-C

97820039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68565434-G-A

97820118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68565372-G-C

http://identifiers.org/hco/15/GRCh38#97820514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68564988-A-C

97820560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68564947-C-G

97820560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68564947-C-T

97820798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68564751-C-T

http://identifiers.org/hco/15/GRCh38#97820845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68564706-C-A

97820892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68564662-T-C

97820892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68564662-T-G

97821155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68564415-C-T

http://identifiers.org/hco/15/GRCh38#97821590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68563989-A-C

97821590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68563989-A-G

97821835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68563786-G-C

97821837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68563784-T-C

97821969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68563656-A-G

http://identifiers.org/hco/15/GRCh38#97822027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68563600-C-A

97822027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68563600-C-T

97822029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68563598-C-T

97822112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68563508-T-C

97837827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68558033-T-C

97837914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68557946-G-C

97838182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68557683-A-G

http://identifiers.org/hco/15/GRCh38#97838217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68557649-C-A

97838381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68557501-C-T

http://identifiers.org/hco/15/GRCh38#97838881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68557061-C-A

http://identifiers.org/hco/15/GRCh38#97838885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68557057-C-A

97838931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68557012-T-G

97838979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68556964-T-C

97839035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68556908-G-T

97839137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68556784-T-A

97839144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68556777-A-G

97839438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68556479-G-C

97839445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68556472-T-A

97839458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68556459-T-A

http://identifiers.org/hco/15/GRCh38#97839626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68556297-C-A

97839626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68556297-C-T

97839958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68555970-T-C

97840621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68555670-C-T

97840653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68555638-A-G

97840711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68555603-G-A

97840793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68555525-T-C

97845517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68544905-T-C

97845802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68544665-A-G

97848080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68544372-A-G

97848262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68544206-A-G

97848711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68543049-G-A

97848833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68542944-G-C

97848833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68542944-G-T

http://identifiers.org/hco/15/GRCh38#97849556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68542456-A-C

97849609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68542404-T-C

97849648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68542372-C-G

97849787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68542238-G-A

97849788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68542237-A-G

97849815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68542209-A-T

97849867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68542158-T-C

97849953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68542065-T-C

97850205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68541824-T-G

97850952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68541738-T-C

97851558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68541123-G-A

97851819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68540428-T-C

97856606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68536690-A-G

97856672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68536618-G-A

http://identifiers.org/hco/15/GRCh38#97856675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68536588-A-C

97856712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68536558-T-A

http://identifiers.org/hco/15/GRCh38#97857022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68536270-C-A

97857022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68536270-C-T

97857235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68536054-C-T

97857472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68535820-A-G

97857475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68535817-C-T

97857651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68535649-T-A

97858106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68534351-T-A

97858106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68534351-T-C

http://identifiers.org/hco/15/GRCh38#97858443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68534040-C-A

97858540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68533945-T-C

97858637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68533846-T-A

97858682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68533801-G-A

97859020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68533469-C-T

97859216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68533271-T-C

97859381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68533105-A-G

97860878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68530262-A-G

97860878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68530262-A-T

97860893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68530247-A-G

97860979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68530121-T-C

97860979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68530121-T-G

97861169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68529699-T-C

97861604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68528747-A-G

http://identifiers.org/hco/15/GRCh38#97861660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68528693-A-C

97861726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68528480-G-A

97861726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68528480-G-C

97861951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68528238-G-C

97862011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68528170-C-G

97862028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68528153-G-C

97862081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68528114-T-C

97864292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68517372-G-A

97864292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68517372-G-C

97864298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68517366-T-C

97864498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68517172-T-C

97864529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68517141-G-A

97864529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68517141-G-T

97864568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68517109-T-C

97864654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68517038-G-A

http://identifiers.org/hco/15/GRCh38#97864980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68516721-C-A

97865004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68516697-T-C

97866051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68515329-G-A

97866083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68515290-T-C

97866228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68515077-C-T

http://identifiers.org/hco/15/GRCh38#97866407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68514933-C-A

http://identifiers.org/hco/15/GRCh38#97866489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68514853-A-C

97866516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68514826-T-C

97866793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68514563-T-C

97866823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68514533-A-G

97866832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68514524-C-T

97866975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68514379-T-C

97867226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68514129-G-A

97867347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68514022-C-T

97867379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68513989-G-A

97867379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68513989-G-C

97867458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68513920-T-C

97867551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68513830-T-C

97867559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68513822-T-C

http://identifiers.org/hco/15/GRCh38#97867591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68513789-C-A

97867848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68513521-C-T

97867852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68513518-G-A

97867857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68513513-G-A

97867921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68513458-T-A

97868479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68512921-G-C

97868665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68512637-T-C

97868665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68512637-T-G

97868713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68512423-G-T

97869224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68511952-G-C

97869273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68511904-G-A

97871079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68510929-G-A

http://identifiers.org/hco/15/GRCh38#97871252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68510781-C-A

http://identifiers.org/hco/15/GRCh38#97871271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68510762-C-A

97871288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68510744-C-T

97871328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68510708-G-A

http://identifiers.org/hco/15/GRCh38#97871346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68510690-C-A

97871446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68510580-G-T

97871549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68510471-A-G

97873267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68509831-T-C

97873334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68509766-A-G

97873421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68509680-T-C

97873434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68509667-G-A

97873440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68509661-C-T

97873544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68509547-T-C

97873731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68509354-A-T

http://identifiers.org/hco/15/GRCh38#97873850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68509254-C-A

97873850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68509254-C-T

97873861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68509242-T-C

http://identifiers.org/hco/15/GRCh38#97873870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68509233-A-C

97873870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68509233-A-T

97873992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68509188-G-T

http://identifiers.org/hco/15/GRCh38#97874028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68509160-A-C

97874030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68509158-C-G

97874077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68509109-G-A

97874134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68509052-G-A

97874135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68509051-G-A

97874135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68509051-G-C

http://identifiers.org/hco/15/GRCh38#97874141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68509045-C-A

97874141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68509045-C-T

97874230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68508938-G-C

97874248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68508922-C-T

97874249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68508921-C-T

97874328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68508838-C-T

http://identifiers.org/hco/15/GRCh38#97874423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68508743-C-A

97874455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68508711-T-G

97874485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: non coding transcript exon variant
orthologous variants: 68508678-G-T

97874581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68508585-T-A

97874581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68508585-T-C

97874816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68508357-T-C

97875050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68508111-C-G

97875071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68508086-A-G

97875098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68508026-A-T

97875160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68507966-C-T

97875215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68507923-T-A

97875246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68507893-T-C

97875409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 68507732-T-C

97875437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 68507706-C-G

97875437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 68507706-C-T

97875449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 68507694-A-G

97875449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28088
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 68507694-A-T