http://identifiers.org/hco/8/GRCh38#86514442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19570096-C-A

86514442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5 prime UTR variant
orthologous variants: 19570096-C-T

http://identifiers.org/hco/8/GRCh38#86514496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19570042-A-C

86514496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 19570042-A-G

http://identifiers.org/hco/8/GRCh38#86514509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19570029-C-A

86514564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19569975-T-G

86514570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19569969-G-T

86514581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 19569957-A-G

86514653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19569889-G-A

86514653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19569889-G-T

86514675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19569867-C-T

86514707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19569829-A-G

86514849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19569726-C-T

86514853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19569722-C-G

http://identifiers.org/hco/8/GRCh38#86514860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#19569711-C-A

86515115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19569515-G-A

http://identifiers.org/hco/8/GRCh38#86515121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19569509-C-A

86515121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19569509-C-T

http://identifiers.org/hco/8/GRCh38#86515213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19569435-C-A

86515226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 19569410-G-C

86515335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 19569313-G-T

http://identifiers.org/hco/8/GRCh38#86515375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19569274-C-A

86515375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 19569274-C-T

http://identifiers.org/hco/8/GRCh38#86515658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19568999-A-C

86516044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, undefined
orthologous variants: 19568767-T-C

86516044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, undefined
orthologous variants: 19568767-T-G

86516093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19568719-T-G

86516282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19568549-C-T

86516722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19568073-T-C

86516722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19568073-T-G

86516950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19567871-T-C

86516996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19567825-T-A

http://identifiers.org/hco/8/GRCh38#86517195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19567378-A-C

86517304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19567284-T-C

86517715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19566418-T-C

http://identifiers.org/hco/8/GRCh38#86517735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19566398-A-C

86517815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19566328-A-G

86518169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19565799-A-G

86518290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19565716-C-T

86518409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19565598-G-A

http://identifiers.org/hco/8/GRCh38#86519481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19564700-A-C

86519967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19564321-C-T

86519991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19564297-C-T

86520186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19564118-A-G

http://identifiers.org/hco/8/GRCh38#86521184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19562289-C-A

86521201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19562272-T-C

86525509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19560086-G-A

86525855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19559802-G-T

86525991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19559659-C-T

86526272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19558466-T-C

86528411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19555614-G-A

86528411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19555614-G-T

86528422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19555603-T-C

86528495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19555527-G-C

86528495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19555527-G-T

86528564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: missense variant
orthologous variants: 19555473-A-G

http://identifiers.org/hco/8/GRCh38#86528762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19555288-C-A

86528845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19554033-T-C

86529129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19553711-G-A

86531013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552443-A-G

86531035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552419-G-A

86531035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552419-G-T

86531097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552369-A-T

http://identifiers.org/hco/8/GRCh38#86531138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19552333-C-A

86531138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552333-C-G

86531138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552333-C-T

http://identifiers.org/hco/8/GRCh38#86531142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19552329-C-A

86531142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552329-C-G

86531142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552329-C-T

86531212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: missense variant
orthologous variants: 19552259-G-A

86531212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: stop gained
orthologous variants: 19552259-G-T

86531248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552229-T-A

86531248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552229-T-C

86531316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552179-A-G

http://identifiers.org/hco/8/GRCh38#86531318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19552177-C-A

86531318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552177-C-T

86531346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552149-T-G

86531364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552131-G-A

86531375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19552124-A-G

86531701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19551635-A-G

86532156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19551072-T-C

http://identifiers.org/hco/8/GRCh38#86532372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19550778-C-A

86532372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19550778-C-T

86532587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 19550579-A-G

http://identifiers.org/hco/8/GRCh38#86532595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19550571-C-A

86532595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19550571-C-T

86532612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19550548-G-A

86532612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19550548-G-C

86532774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19550373-T-A

86532835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19550331-A-G

86532872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19550298-A-T

86532924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19550246-C-G

86537283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19543589-A-G

86537402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19543503-T-G

86537410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19543495-T-C

86537417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19543488-G-T

86537471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19543427-A-G

86537482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19543397-A-G

86537494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19543385-G-A

86537494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19543385-G-T

86537665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19543234-A-G

86537678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19543221-G-A

86537678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19543221-G-T

86537720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19543188-A-G

86537931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19543022-G-C

http://identifiers.org/hco/8/GRCh38#86537954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19542991-C-A

86537968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19542977-C-G

86538006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19542939-C-G

86538585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19542559-T-G

86538647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19542496-C-T

http://identifiers.org/hco/8/GRCh38#86538940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19542252-C-A

http://identifiers.org/hco/8/GRCh38#86538989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19542172-A-C

86538989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19542172-A-G

86539561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19541375-A-G

86540014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19541039-A-T

86540083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19540971-T-C

86540163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19540900-G-A

86540349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19540723-T-C

86540365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19540658-T-C

http://identifiers.org/hco/8/GRCh38#86540374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19540530-C-A

86540374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19540530-C-T

http://identifiers.org/hco/8/GRCh38#86540385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19540519-C-A

86540385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19540519-C-T

86540561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19540165-A-G

86540562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19540164-G-A

86540602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19540127-G-T

86540644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19540085-T-C

86540747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19539987-C-T

86540927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19539890-G-T

86541064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19539728-C-G

http://identifiers.org/hco/8/GRCh38#86541205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19539602-A-C

86542683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19538715-G-C

86542684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19538714-G-A

86543429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19538010-A-G

86543600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19537597-G-A

86543600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19537597-G-C

86543781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19537420-A-G

86544145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19537149-C-T

86544555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19536780-G-C

86544600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19536735-C-T

86544675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19536678-T-C

http://identifiers.org/hco/8/GRCh38#86544677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19536676-C-A

86544677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19536676-C-T

86544770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19536593-T-C

86544871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19536494-A-G

http://identifiers.org/hco/8/GRCh38#86545063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19536323-C-A

86545135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19536268-T-C

86545135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19536268-T-G

86545165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19536247-A-G

86545188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19536226-G-A

86545188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19536226-G-C

86545211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19536205-G-A

http://identifiers.org/hco/8/GRCh38#86545245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19536171-C-A

86545337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19536087-G-A

86545337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19536087-G-T

86545346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19536075-A-G

86545360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19536063-C-T

86545418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19536007-G-T

86545425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron variant
orthologous variants: 19536001-T-C

86547205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19534817-A-T

86547206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19534816-G-A

http://identifiers.org/hco/8/GRCh38#86547568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19533258-C-A

http://identifiers.org/hco/8/GRCh38#86547604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19533220-A-C

86547604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19533220-A-G

86547604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19533220-A-T

86547607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19533217-A-G

86547607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19533217-A-T

86547623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19533201-A-G

86547640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19533184-T-A

86547640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19533184-T-C

86547675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19533149-G-A

86547800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19533025-G-A

86547800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19533025-G-T

86547820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532990-A-G

http://identifiers.org/hco/8/GRCh38#86547871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19532943-C-A

86547871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532943-C-T

http://identifiers.org/hco/8/GRCh38#86547918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19532907-C-A

86547918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532907-C-T

86548059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532781-C-T

86548153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532692-T-C

http://identifiers.org/hco/8/GRCh38#86548197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19532640-C-A

86548197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532640-C-T

http://identifiers.org/hco/8/GRCh38#86548225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19532614-C-A

86548225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532614-C-G

http://identifiers.org/hco/8/GRCh38#86548260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19532575-C-A

86548260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532575-C-T

86548448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532383-T-G

86548518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532312-A-G

86548518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532312-A-T

http://identifiers.org/hco/8/GRCh38#86548549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19532289-C-A

86548549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532289-C-G

http://identifiers.org/hco/8/GRCh38#86548560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19532281-C-A

86548617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532224-A-G

86548772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532095-G-A

86548802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532073-T-C

86548838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19532042-T-C

86551023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19528265-A-G

86551026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19528262-A-G

86551211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19528081-A-G

86551334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19527997-A-G

86551422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19527914-G-A

86551504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19527845-T-A

86551610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19527738-G-A

86551610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19527738-G-T

http://identifiers.org/hco/8/GRCh38#86551656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19527692-C-A

86551656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19527692-C-T

http://identifiers.org/hco/8/GRCh38#86551658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19527690-C-A

86551658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19527690-C-G

86551658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19527690-C-T

86553881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19527387-G-C

86553885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19527383-G-A

86553885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19527383-G-T

86553887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19527381-G-C

86553887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19527381-G-T

http://identifiers.org/hco/8/GRCh38#86553909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19527360-C-A

86553909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19527360-C-T

86553936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19527333-C-T

86554005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19527265-T-C

86554053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19527216-A-G

86554305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19526990-C-T

86554415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19526888-C-G

86554415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19526888-C-T

86554573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19526779-G-T

86554686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19526689-A-G

86554718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19526680-T-C

86554767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19526569-A-G

86554768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19526568-T-C

86554871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19526395-G-A

86554901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19526365-C-T

86555019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19526249-T-C

86555028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19526244-A-G

http://identifiers.org/hco/8/GRCh38#86555042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19526226-C-A

http://identifiers.org/hco/8/GRCh38#86555050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19526218-C-A

86555389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19525884-A-G

86555412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19525869-T-C

86555490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19525779-G-T

86555619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19525649-T-A

http://identifiers.org/hco/8/GRCh38#86556032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19525309-C-A

86556032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19525309-C-T

86556040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19525301-G-A

86556040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19525301-G-T

86556196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19525143-C-G

86556264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19525075-A-G

86556276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19525063-C-T

86556282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19525057-G-A

http://identifiers.org/hco/8/GRCh38#86558164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19523562-A-C

86558164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19523562-A-G

86558164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19523562-A-T

86558174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19523552-C-G

http://identifiers.org/hco/8/GRCh38#86558235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19523345-A-C

86558294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19523286-A-G

http://identifiers.org/hco/8/GRCh38#86558362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/4/GRCm39#19523218-C-A

86558456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19523129-C-T

http://identifiers.org/hco/8/GRCh38#86558490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19523098-C-A

http://identifiers.org/hco/8/GRCh38#86558502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19523086-A-C

86558502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19523086-A-G

86558640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19522947-G-A

86558699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19522889-T-C

86558815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19522779-A-G

86559387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19522167-T-A

86559387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19522167-T-C

http://identifiers.org/hco/8/GRCh38#86559756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19521798-A-C

86559793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19521761-A-G

86559828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19521733-A-G

http://identifiers.org/hco/8/GRCh38#86559965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19521637-C-A

86559986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19521616-G-A

86560037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19521569-G-T

http://identifiers.org/hco/8/GRCh38#86560162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19520293-C-A

86560162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19520293-C-T

86560385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19520083-T-C

86560446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19520045-C-T

86561079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19519524-C-T

http://identifiers.org/hco/8/GRCh38#86561126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#19519477-C-A

86561373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19519289-A-G