http://identifiers.org/hco/12/GRCh38#65761016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120375013-C-A

65761016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120375013-C-T

65761041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120374988-G-C

65761122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120374934-A-G

65761298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120374778-C-T

http://identifiers.org/hco/12/GRCh38#65761635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120374428-A-C

65761937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120374136-A-G

65761961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120374113-G-A

65761975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120374099-G-T

65762158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120373939-A-G

http://identifiers.org/hco/12/GRCh38#65762185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120373911-C-A

65762284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120373822-G-A

65762284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120373822-G-T

65763020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120373459-A-T

65763077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120373422-C-T

65763149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120373354-C-T

65763211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120373282-A-G

65763484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120373044-C-T

65763592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120372936-G-A

65763592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120372936-G-T

65763615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120372913-G-C

65763621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120372907-C-T

65763943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120372578-T-G

65764049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120372494-C-T

65764171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120372372-C-T

65764262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120372251-T-C

65764352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120372168-T-C

65764492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120372038-G-T

65764549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120371937-G-A

65764567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120371817-A-G

http://identifiers.org/hco/12/GRCh38#65764764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120371542-A-C

65764764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120371542-A-G

http://identifiers.org/hco/12/GRCh38#65766372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120370089-C-A

65766791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120369657-G-A

65766979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120369519-G-A

65766991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120369507-T-C

65767085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120369406-G-T

http://identifiers.org/hco/12/GRCh38#65767096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120369395-C-A

65767156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120369334-A-G

65767173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120369315-A-G

65767265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120369223-A-G

65767338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120369144-A-G

65767438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120369042-T-C

65767524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120368943-C-T

65768109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120368280-G-C

65772228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120367535-A-G

65772228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120367535-A-T

65772538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120367159-C-T

65772751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120366958-T-G

65772798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120366912-A-G

65772915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120366810-T-C

65772925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120366800-C-T

65773003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120366708-T-C

65773004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120366707-G-A

65773041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120366677-C-G

http://identifiers.org/hco/12/GRCh38#65773075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120366292-C-A

65773075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120366292-C-T

65773945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120365347-G-A

http://identifiers.org/hco/12/GRCh38#65774059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120365234-A-C

65774565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120364884-A-G

65774638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120364814-A-G

65774934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120364526-G-A

65774938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120364522-G-A

65774978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120364488-C-G

65774997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120364469-G-T

65775081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120364432-A-T

65776806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120363416-A-T

65776849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120363374-C-T

65776859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120363369-G-A

65776884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120363353-T-C

65777167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120363070-T-A

65777520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120362724-T-C

65777652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120362619-G-A

65778205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120362244-T-C

65778285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120362213-T-C

http://identifiers.org/hco/12/GRCh38#65778417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120362165-C-A

65778495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120362090-G-T

http://identifiers.org/hco/12/GRCh38#65778511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120362073-A-C

65778551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120362033-G-T

65778638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120361945-A-G

65778721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120361866-T-C

65778725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120361860-G-A

65778725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120361860-G-C

65778963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120361775-C-G

65779071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120361739-C-G

65779071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120361739-C-T

65779086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120361724-C-T

65779141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120361669-C-G

http://identifiers.org/hco/12/GRCh38#65779254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#120361560-C-A

65779295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120361519-A-T

65779352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120361498-T-C

65779459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120361393-G-T

65781121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120358381-G-A

65781128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120358374-C-T

65781217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120358286-G-A

65781252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120358251-C-T

65781926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120357566-C-T

65782127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120357392-T-G

65782163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120357358-C-G

65784140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120354425-T-G

65789993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120351039-T-C

65790378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120350313-A-G

65790411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120350279-G-T

65790460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120350231-A-G

65790460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120350231-A-T

65790492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120350199-A-G

65790560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120350147-A-T

65790611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120350096-T-A

65790658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120350079-G-C

65791106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120349667-C-T

65791136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120349635-G-T

65791383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120349340-T-A

65791433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120349295-T-G

65791568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120349161-G-A

http://identifiers.org/hco/12/GRCh38#65791868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120348877-C-A

65791868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120348877-C-T

65791947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120348765-A-G

65792046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120348412-C-T

65792061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120348397-A-T

65792124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120348332-G-C

65792242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120348214-A-T

http://identifiers.org/hco/12/GRCh38#65792445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120347994-A-C

65792445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120347994-A-G

65792706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120347753-T-C

65792875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120347362-A-G

65792969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120347280-T-C

65793004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120347249-G-A

65793014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120347239-T-A

65793014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120347239-T-C

65793451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120346753-T-C

http://identifiers.org/hco/12/GRCh38#65793638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120346600-C-A

65793701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120346537-G-T

65793804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120346362-T-C

65793903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120346186-A-G

65795323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120345340-G-T

65795411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120345254-C-T

65796549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120344292-C-T

65796730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120344116-T-C

65796814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120344041-A-G

65796882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120343974-A-G

65797319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120342370-A-G

http://identifiers.org/hco/12/GRCh38#65797343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120342345-C-A

65797343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120342345-C-T

http://identifiers.org/hco/12/GRCh38#65797370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120342317-C-A

65797456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120342223-G-T

65798049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120340756-C-T

65798186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120340669-G-A

65798636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120340270-C-T

65798667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120340243-G-A

http://identifiers.org/hco/12/GRCh38#65798726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120340183-C-A

65798726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120340183-C-G

65799100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120339846-C-T

65799101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120339845-T-C

65799173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120339743-C-T

65799347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120339557-C-G

65799612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120339317-G-A

65799640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120339287-A-G

65799860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120339085-C-T

http://identifiers.org/hco/12/GRCh38#65799881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120339063-C-A

65799881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120339063-C-T

65799981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120338967-A-G

65799993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120338961-T-C

65800078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120338884-A-T

65800095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120338867-G-A

65800095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120338867-G-T

65801138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120337563-A-G

http://identifiers.org/hco/12/GRCh38#65801416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120337249-C-A

65801436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120337229-A-G

65801447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120337218-G-A

65801499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120337169-C-T

65802057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120336092-A-T

65802934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120334490-A-G

65803097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120334305-C-T

65803190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120334208-A-G

http://identifiers.org/hco/12/GRCh38#65803284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120334112-C-A

65803301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120334095-A-G

http://identifiers.org/hco/12/GRCh38#65805135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120330679-A-C

65808314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120327993-T-A

65808369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120327948-C-T

http://identifiers.org/hco/12/GRCh38#65808374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120327943-A-C

65808374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120327943-A-T

65808384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120327933-T-G

65808503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120327779-A-G

http://identifiers.org/hco/12/GRCh38#65808554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120327727-C-A

65808648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120327663-T-C

65808674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120327637-G-A

65808684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120327627-T-G

65808735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120327576-C-T

65808762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120327549-G-C

65808818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120327492-A-T

65808996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120327330-C-T

65809110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120327217-A-G

65809136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120327192-C-T

65809498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120326261-A-G

65809556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120326236-A-G

65809880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120326027-G-A

65810351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120325548-C-T

65810374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120325526-C-T

65810689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120325245-G-A

65821061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120316465-G-A

65821120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120316281-G-A

65821181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120316217-G-A

65821181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120316217-G-T

65821902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120315583-T-C

65821934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120315551-C-T

65822062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120315464-C-G

65822131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120315414-A-G

65822687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120314693-C-G

65822925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120314372-C-T

65823079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120314217-A-G

65823104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120314192-G-A

65823104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120314192-G-T

65823342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313939-G-A

65823589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313712-G-T

65823671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120313628-G-A

65823753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313525-G-C

65823859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313422-A-G

http://identifiers.org/hco/12/GRCh38#65823982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120313292-C-A

65823982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313292-C-T

http://identifiers.org/hco/12/GRCh38#65824078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120313197-C-A

65824091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313184-G-A

65824147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313149-G-A

http://identifiers.org/hco/12/GRCh38#65824160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#120313135-A-C

65824164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120313131-C-T

http://identifiers.org/hco/12/GRCh38#65824228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120313067-C-A

65824228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313067-C-G

65824228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313067-C-T

65824283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120313012-T-G

65824399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312900-G-A

65824399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312900-G-C

65824399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312900-G-T

http://identifiers.org/hco/12/GRCh38#65824585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#120312733-C-A

65824585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312733-C-T

65824654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312659-G-A

http://identifiers.org/hco/12/GRCh38#65824733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#120312579-C-A

65824733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312579-C-G

65824741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312540-C-G

65825130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312136-G-A

65825130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312136-G-T

http://identifiers.org/hco/12/GRCh38#65825144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#120312117-C-A

65825144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312117-C-T

65825178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312078-G-A

65825178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312078-G-T

65825207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312048-T-C

65825207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312048-T-G

65825233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312022-A-G

65825233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120312022-A-T

65825392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311845-G-A

65825392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311845-G-T

http://identifiers.org/hco/12/GRCh38#65825448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#120311784-C-A

65825448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311784-C-T

65825477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311755-G-A

65825477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311755-G-T

65825662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311556-C-T

65825687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311530-C-T

65825788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311447-G-T

65825801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311434-G-A

65825801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311434-G-T

65825816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311419-G-A

65825816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311419-G-C

65825907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311332-G-A

65825907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311332-G-T

65825986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311249-T-C

65826004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311221-T-C

65826011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311214-G-A

65826011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311214-G-T

http://identifiers.org/hco/12/GRCh38#65826032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#120311195-C-A

65826032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311195-C-T

65826090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311137-C-T

http://identifiers.org/hco/12/GRCh38#65826118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#120311119-C-A

65826118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311119-C-T

65826178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311059-G-A

65826178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311059-G-T

65826188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311049-G-A

http://identifiers.org/hco/12/GRCh38#65826189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#120311048-C-A

65826189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311048-C-G

65826189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311048-C-T

65826214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120311025-A-G

65826348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120310891-G-A

65826348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120310891-G-T

http://identifiers.org/hco/12/GRCh38#65826679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#120310551-A-C

http://identifiers.org/hco/12/GRCh38#65826692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#120310538-C-A

65826728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120310502-C-G

http://identifiers.org/hco/12/GRCh38#65826730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#120310501-A-C

65826730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120310501-A-G

65826730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120310501-A-T

http://identifiers.org/hco/12/GRCh38#65826762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#120310464-C-A

65826818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120310418-G-A

65826825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120310411-G-A