http://identifiers.org/hco/1/GRCh38#110150567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107425251-C-A

110150622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 5 prime UTR variant
orthologous variants: 107425198-T-C

110150723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 5 prime UTR variant
orthologous variants: 107425097-G-A

110150723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 5 prime UTR variant
orthologous variants: 107425097-G-C

110150724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 107425096-A-G

110150724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 107425096-A-T

http://identifiers.org/hco/1/GRCh38#110150814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107424989-C-A

110150926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107424877-C-T

110150969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107424835-G-A

110150969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107424835-G-C

http://identifiers.org/hco/1/GRCh38#110151015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107424794-C-A

110151015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107424794-C-T

110151019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107424790-G-A

110151195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107424616-T-G

110151323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107424491-T-C

http://identifiers.org/hco/1/GRCh38#110151506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107424312-C-A

110152119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107423750-G-A

110152672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107423256-C-T

http://identifiers.org/hco/1/GRCh38#110152712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107423216-A-C

http://identifiers.org/hco/1/GRCh38#110152722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107423206-C-A

110152763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107423169-G-A

110153061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107422866-G-A

110153391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107422566-C-T

http://identifiers.org/hco/1/GRCh38#110153461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107422375-C-A

110153719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107422125-A-G

110153797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107422047-T-C

110153815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107422022-C-T

110153867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107421970-C-T

110153870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107421967-C-T

110153883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107421955-A-G

110154071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107421586-T-C

110154071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107421586-T-G

110154088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107421569-G-A

110154212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107421446-T-C

110154281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107421378-A-G

110154374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107421273-T-C

110154507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107421137-C-T

110154710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107420934-G-A

http://identifiers.org/hco/1/GRCh38#110155174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107420484-A-C

110155175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107420483-C-T

110155198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107420453-C-T

110155207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107420444-C-G

110155207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107420444-C-T

110155260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107420390-T-A

110155339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107420315-A-G

110155396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107420258-T-G

110155494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107420158-G-C

110155701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107420021-C-G

110155708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107420014-C-T

110155775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107419956-C-T

110155815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107419915-C-T

http://identifiers.org/hco/1/GRCh38#110155818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107419912-A-C

110155953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, undefined
orthologous variants: 107419789-G-A

110156186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, undefined
orthologous variants: 107419569-G-T

110156978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107418524-A-G

110157146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107418374-C-T

110157842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107417993-A-G

http://identifiers.org/hco/1/GRCh38#110158099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107417851-C-A

110158099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107417851-C-G

110158171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107417778-C-T

110158609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107417392-T-C

110158716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107417282-C-G

110158846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107417183-C-T

110158923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107417118-T-A

110158973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107417093-G-A

110159756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107415825-G-C

110160167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107415461-T-A

110160273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107415358-C-G

110160296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107415335-G-T

110160922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107414499-G-A

110161017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107414403-C-T

110161102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107414316-C-T

110161190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107414224-C-T

http://identifiers.org/hco/1/GRCh38#110161435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107413989-C-A

110161777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107413717-G-A

110161819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107413678-C-T

http://identifiers.org/hco/1/GRCh38#110161899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107413600-C-A

110161899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107413600-C-G

110161945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107413554-A-G

110162367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107413123-T-C

http://identifiers.org/hco/1/GRCh38#110163020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107412246-A-C

110163020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107412246-A-T

110163064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107412200-T-C

110163499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107411649-G-T

110163516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107411632-A-T

110163606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107411546-T-G

110163673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107411480-A-G

http://identifiers.org/hco/1/GRCh38#110163958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107411192-C-A

110163958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107411192-C-T

http://identifiers.org/hco/1/GRCh38#110164429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107410824-C-A

110164581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107410667-C-G

110164581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107410667-C-T

110164621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107410626-G-A

110164670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107410583-A-G

110164698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107410548-G-T

110164854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107410410-C-G

110165167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107410087-C-G

110165253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107410009-C-T

110165315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107409954-G-A

110165441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107409834-C-T

110165465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107409805-T-C

110165532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107409736-T-C

110165535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107409733-G-A

110165569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107409699-C-T

110165654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107409598-C-G

110165808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107409455-A-G

110166104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107409153-C-T

110166262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107408995-C-T

110166556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107408346-T-G

110166583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107408320-G-A

110166605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107408298-G-T

http://identifiers.org/hco/1/GRCh38#110166606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107408297-C-A

110166678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107408219-T-A

http://identifiers.org/hco/1/GRCh38#110166684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107408213-C-A

110166684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107408213-C-T

110166711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107408189-G-A

110166718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107408182-G-A

110166718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107408182-G-C

110166718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107408182-G-T

110166752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107408156-G-A

110166912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107407985-A-G

110166912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107407985-A-T

110166957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107407940-C-T

110166981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107407916-A-G

110166990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107407907-G-A

110166990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107407907-G-C

110167104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107407793-G-A

110167375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107407523-A-G

110167504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107407365-A-G

110168249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107406231-A-G

110169668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107405161-G-A

110169842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107405006-G-A

110169843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107405005-T-C

110169850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107404998-G-A

110169979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107404891-G-A

110170517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107404693-C-T

110170560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107404655-C-T

110170903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107404296-C-T

110170993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107404228-G-T

110171383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107403854-C-T

110171706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107403529-C-T

110171710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107403525-G-A

110171722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107403513-G-A

http://identifiers.org/hco/1/GRCh38#110171960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107403305-C-A

110171960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107403305-C-T

110171979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107403286-G-A

http://identifiers.org/hco/1/GRCh38#110172023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107403175-C-A

110172023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107403175-C-T

110172411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107402788-A-G

110172411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107402788-A-T

http://identifiers.org/hco/1/GRCh38#110172425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107402774-A-C

http://identifiers.org/hco/1/GRCh38#110172534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107402676-C-A

110172538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107402665-G-T

http://identifiers.org/hco/1/GRCh38#110172543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107402660-C-A

110172543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107402660-C-T

http://identifiers.org/hco/1/GRCh38#110172544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107402659-C-A

110172550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107402641-T-C

110172563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107402629-C-T

110172583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107402616-G-A

110172784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107402465-T-C

110172998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107402264-C-G

110173053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107402240-A-G

110173068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107402225-A-G

110173566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401758-G-C

110173601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401729-C-T

110173637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401695-C-T

http://identifiers.org/hco/1/GRCh38#110173831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107401501-C-A

110173831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401501-C-T

110173895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401457-G-A

110173895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401457-G-C

110173895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401457-G-T

110173905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401447-G-A

110173905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401447-G-C

110173905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401447-G-T

http://identifiers.org/hco/1/GRCh38#110173913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107401439-C-A

110173913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401439-C-G

110173913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401439-C-T

110173917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401435-G-A

110173917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401435-G-T

110173925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401429-G-A

110174107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 107401243-T-G

110174117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401221-C-G

110174151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401187-G-T

http://identifiers.org/hco/1/GRCh38#110174153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107401185-C-A

http://identifiers.org/hco/1/GRCh38#110174168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107401170-C-A

110174168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107401170-C-T

110174308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107400990-G-C

110174338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107400963-T-G

110174505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107400803-C-T

110174520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107400788-A-T

110174570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107400740-T-C

110174699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107400640-G-A

110174699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107400640-G-T

http://identifiers.org/hco/1/GRCh38#110174700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107400639-C-A

110174713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107400627-T-C

110174713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107400627-T-G

110174722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107400618-G-T

http://identifiers.org/hco/1/GRCh38#110174987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107400367-C-A

110174987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107400367-C-T

110174988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107400366-C-G

110175055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107400313-G-A

110175055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107400313-G-T

110175468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107399960-A-G

110175674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107399782-G-A

110175779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107399645-C-G

110175779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107399645-C-T

110175926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107399503-G-A

110175993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107399433-A-G

110176311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107399133-G-C

110176339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107399105-C-T

110176410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, undefined
orthologous variants: 107399058-C-G

http://identifiers.org/hco/1/GRCh38#110176508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107398967-C-A

110176508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, undefined
orthologous variants: 107398967-C-T

110176557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107398914-T-G

110176576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107398895-T-C

http://identifiers.org/hco/1/GRCh38#110176582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107398889-C-A

110176582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107398889-C-G

110176594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107398877-C-T

110176683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: missense variant
orthologous variants: 107398790-C-T

110176716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: missense variant
orthologous variants: 107398757-A-G

http://identifiers.org/hco/1/GRCh38#110176838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107398641-C-A

110176855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107398624-A-G

110176869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107398610-T-A

110176869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107398610-T-C

110177355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107398161-T-A

110177386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107398139-G-C

110177439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107398086-C-T

110177620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107397946-A-G

http://identifiers.org/hco/1/GRCh38#110177909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107397636-C-A

110177909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107397636-C-T

110177980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107397581-C-T

110178022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107397554-G-A

110178504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107397091-A-T

110178637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107396959-G-C

110178637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107396959-G-T

110178658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107396938-G-A

110178809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107396717-C-G

http://identifiers.org/hco/1/GRCh38#110178814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107396713-C-A

110178909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107396654-T-C

110178997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107396574-T-A

110179896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107395693-A-G

110180020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107395588-G-A

110180230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107395512-T-A

110180246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107395496-G-T

110180261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107395482-G-A

110180651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107395272-A-G

110180763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107395149-T-C

110180849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107395062-G-T

http://identifiers.org/hco/1/GRCh38#110180931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107394999-A-C

110181086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107394845-G-A

110181222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107394716-C-T

110181414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107394532-A-G

110181435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107394507-C-T

110181463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107394485-G-A

110181463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107394485-G-T

110181648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107394315-G-A

110181768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107394193-C-T

110182197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107393857-G-A

110182200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107393854-G-A

110182200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107393854-G-C

110182380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107393681-T-C

110182397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107393668-A-T

110182443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107393623-A-G

110182575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107393499-G-A

http://identifiers.org/hco/1/GRCh38#110183268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107392800-A-C

110183268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107392800-A-G

110183268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107392800-A-T

110184595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107391533-G-A

110184646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107391487-C-T

110184683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107391451-G-A

110184800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107391368-A-T

110184943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107391221-G-A

110184981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107391182-C-G

110185110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107391074-C-G

110185289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107390919-T-C

110185335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107390873-G-A

http://identifiers.org/hco/1/GRCh38#110185494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107390689-A-C

http://identifiers.org/hco/1/GRCh38#110191353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107384975-C-A

110191353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107384975-C-T

110191832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107384879-T-C

http://identifiers.org/hco/1/GRCh38#110192315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107384402-C-A

110192432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107384297-G-T

http://identifiers.org/hco/1/GRCh38#110192485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107384255-C-A

110192486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107384254-C-T

110192702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107384038-C-G

110192702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107384038-C-T

110192765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383977-C-G

110192765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383977-C-T

110192834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383911-G-A

110192834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383911-G-T

110192905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383848-A-G

110193065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383467-T-C

110193073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383453-C-T

110193279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383238-C-T

110193320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107383199-G-A

http://identifiers.org/hco/1/GRCh38#110193778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107382690-C-A

110194285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107382229-A-G

110194316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107382202-A-T

http://identifiers.org/hco/1/GRCh38#110194332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107382187-C-A

http://identifiers.org/hco/1/GRCh38#110194432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107381916-C-A

110194432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381916-C-T

http://identifiers.org/hco/1/GRCh38#110194433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107381915-C-A

110194433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381915-C-T

110194438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381910-T-C

http://identifiers.org/hco/1/GRCh38#110194555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107381802-C-A

110194555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107381802-C-T

http://identifiers.org/hco/1/GRCh38#110194572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107381785-C-A

110194572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107381785-C-T

110194654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107381703-T-C

110194783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107381574-C-T

110194846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107381519-C-T

http://identifiers.org/hco/1/GRCh38#110194853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107381512-C-A

110194853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107381512-C-T

110194910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107381464-G-A

110194910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107381464-G-T

110194934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107381440-T-A

110194934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107381440-T-C

http://identifiers.org/hco/1/GRCh38#110195023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107381415-C-A

http://identifiers.org/hco/1/GRCh38#110195261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107381335-A-C

110195261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107381335-A-G

110195316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107381280-G-A

110195316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107381280-G-T

110195467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107381129-G-A

110195467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107381129-G-T

110195539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107381065-C-T

http://identifiers.org/hco/1/GRCh38#110195563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107381032-A-C

110195767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107380828-G-C

http://identifiers.org/hco/1/GRCh38#110195824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107380736-A-C

110196079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107380485-C-T

110196147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107380442-T-A

110196147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107380442-T-C

110196238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107380369-C-G

http://identifiers.org/hco/1/GRCh38#110196322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107380297-C-A

110196322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107380297-C-T

110196336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107380283-T-C

http://identifiers.org/hco/1/GRCh38#110196746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107380113-C-A

110196746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107380113-C-G

http://identifiers.org/hco/1/GRCh38#110196893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107379977-C-A

110197260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107379654-G-A

110197318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107379612-A-G

http://identifiers.org/hco/1/GRCh38#110197326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107379604-C-A

110197326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107379604-C-T

110197370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107379577-G-A

110197370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107379577-G-T

110197504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: missense variant
orthologous variants: 107379445-T-C

http://identifiers.org/hco/1/GRCh38#110197613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107379336-C-A

110197613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107379336-C-G

110197613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107379336-C-T

110197632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107379315-T-C

110197645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107379302-G-A

110197645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107379302-G-T

http://identifiers.org/hco/1/GRCh38#110197701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107379249-C-A

http://identifiers.org/hco/1/GRCh38#110197705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107379245-C-A

110197705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107379245-C-T

110197958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107378972-G-A

110197958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107378972-G-T

110197961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107378969-G-A

110197961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: intron variant
orthologous variants: 107378969-G-T

110198185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: missense variant
orthologous variants: 107378754-A-G

110198310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: missense variant
orthologous variants: 107378629-G-A

110198370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: missense variant
orthologous variants: 107378569-G-A

110198370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: stop gained
orthologous variants: 107378569-G-T

http://identifiers.org/hco/1/GRCh38#110198424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107378515-A-C

http://identifiers.org/hco/1/GRCh38#110198491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107378450-C-A

110198491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107378450-C-G

110198491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107378450-C-T

110198700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107378252-A-G

110198700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107378252-A-T

http://identifiers.org/hco/1/GRCh38#110198791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107378182-C-A

110198791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107378182-C-G

110198791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107378182-C-T

110198823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107378148-T-C

110198823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107378148-T-G

http://identifiers.org/hco/1/GRCh38#110198846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107378100-A-C

110198888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107378056-T-C

110198931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107378017-G-A

110198931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107378017-G-T

110198970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377997-G-A

110198970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377997-G-T

110198971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377996-G-A

110198971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377996-G-T

110199075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377889-G-T

110199083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377881-G-A

110199085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377879-A-G

110199183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377816-G-A

110199183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377816-G-C

110199183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377816-G-T

110199236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377776-A-G

110199236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377776-A-T

http://identifiers.org/hco/1/GRCh38#110199316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107377693-C-A

110199316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377693-C-T

110199346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377659-G-T

110199457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377557-G-T

110199587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377428-T-G

http://identifiers.org/hco/1/GRCh38#110199617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107377398-C-A

110199617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377398-C-T

110199624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377390-G-T

110199635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377379-G-A

110199635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377379-G-T

110199641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377373-G-A

110199664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377350-T-G

http://identifiers.org/hco/1/GRCh38#110199751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107377297-C-A

110199828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377211-T-C

110199843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377185-G-A

110199843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377185-G-C

110199843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377185-G-T

110199877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377162-G-T

110199880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107377159-A-G

110200137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376886-A-G

110200140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376883-G-T

110200143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376877-A-G

110200150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376870-A-G

110200170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376850-C-T

http://identifiers.org/hco/1/GRCh38#110200283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107376733-A-C

110200283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376733-A-G

http://identifiers.org/hco/1/GRCh38#110200677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107376329-C-A

110200677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376329-C-T

http://identifiers.org/hco/1/GRCh38#110200694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107376312-C-A

110200694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376312-C-T

110200758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376222-A-G

http://identifiers.org/hco/1/GRCh38#110200771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107376209-C-A

110200771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376209-C-T

110200775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376197-G-A

110200779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376193-G-A

110200779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376193-G-T

110200813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376154-G-A

110200813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107376154-G-T

110201203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375801-T-C

110201224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375778-G-A

110201226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375776-C-T

http://identifiers.org/hco/1/GRCh38#110201241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107375761-C-A

110201241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375761-C-G

110201263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375747-G-T

110201297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375716-A-G

http://identifiers.org/hco/1/GRCh38#110201305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107375709-C-A

110201323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375690-G-T

110201354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375666-A-G

110201362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375658-T-C

http://identifiers.org/hco/1/GRCh38#110201409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107375616-C-A

110201464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375558-T-C

110201469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375550-T-C

http://identifiers.org/hco/1/GRCh38#110201485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107375535-C-A

110201485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375535-C-G

110201614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375403-C-T

110201672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375341-A-G

110201687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375328-T-C

110201738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375288-C-T

http://identifiers.org/hco/1/GRCh38#110201789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107375239-C-A

http://identifiers.org/hco/1/GRCh38#110201797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107375231-C-A

110201799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375229-C-T

110201950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107375110-T-C

110202123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: 107374939-G-T

http://identifiers.org/hco/1/GRCh38#110202148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107374914-C-A