77697725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5 prime UTR variant
orthologous variants: 103887684-T-G

77697734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 103887693-G-A

77697734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 103887693-G-T

http://identifiers.org/hco/13/GRCh38#77697952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#103887829-C-A

77697952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 103887829-C-G

77697952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 103887829-C-T

77697976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103887853-G-A

77697976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103887853-G-C

77697976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103887853-G-T

http://identifiers.org/hco/13/GRCh38#77698139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103888018-C-A

77698139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, stop_gained
orthologous variants: 103888018-C-T

77698174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103888054-G-A

77698174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103888054-G-T

77698216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103888075-G-A

77698216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103888075-G-C

77698216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103888075-G-T

77698373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, missense_variant
orthologous variants: 103888181-G-A

77698373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, missense_variant
orthologous variants: 103888181-G-T

http://identifiers.org/hco/13/GRCh38#77698384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103888192-C-A

77698384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, missense_variant
orthologous variants: 103888192-C-G

77698384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103888192-C-T

77698413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, missense_variant
orthologous variants: 103888218-G-A

77698413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, missense_variant
orthologous variants: 103888218-G-C

77698413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, missense_variant
orthologous variants: 103888218-G-T

77698414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103888219-G-A

77698414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103888219-G-T

77698482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 103888287-T-C

http://identifiers.org/hco/13/GRCh38#77698510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103888315-C-A

77698510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 103888315-C-T

http://identifiers.org/hco/13/GRCh38#77698559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103888364-C-A

77698559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103888364-C-G

77698559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103888364-C-T

77698746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103888498-T-C

77698900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103888642-G-A

77698900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103888642-G-C

77698900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103888642-G-T

77698928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 103888685-T-G

77698930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 103888687-G-A

77698930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 103888687-G-T

http://identifiers.org/hco/13/GRCh38#77698981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103888742-C-A

77698981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 103888742-C-G

77698981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 103888742-C-T

77698998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 103888759-G-A

77699016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, stop_gained
orthologous variants: 103888776-G-A

http://identifiers.org/hco/13/GRCh38#77699065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103888821-C-A

77699172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103888921-T-C

77699243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103888982-T-G

77699249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103888988-A-G

77699249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103888988-A-T

77699293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103889019-T-A

77699320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103889496-A-G

77699320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103889496-A-T

77699371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103889545-C-T

77699621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103889967-C-T

77699701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103890043-A-G

77699854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103890198-T-C

77700019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103890350-A-G

77700079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103890404-T-C

77700126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103890495-G-C

77700308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103890774-A-T

77700343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103890809-A-G

77700353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103890819-A-G

77700513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103890985-A-G

77715928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103891387-A-G

77715988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103891451-T-A

77716128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103891589-T-G

77716131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103891592-T-G

77716134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103891595-T-C

77716135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103891596-C-G

77716135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103891596-C-T

http://identifiers.org/hco/13/GRCh38#77716160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103891598-C-A

77716160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103891598-C-T

77716216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103891657-C-T

77716286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103891735-T-G

77716302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103891751-A-T

http://identifiers.org/hco/13/GRCh38#77716357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103891791-C-A

77716514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103891978-A-G

77716937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103892346-C-G

77717099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103892502-T-A

77717100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103892503-A-G

77717143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103892562-G-A

77717220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103892634-C-T

http://identifiers.org/hco/13/GRCh38#77717580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103892994-C-A

77717631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103893006-C-G

77717631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103893006-C-T

77717665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103893040-G-A

77717665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103893040-G-T

77717946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103893314-A-G

77718394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103893806-G-A

http://identifiers.org/hco/13/GRCh38#77719325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103894157-C-A

77719404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103894238-G-T

77719430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103894263-T-G

77719574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 103894411-A-T

77719682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103894518-G-A

77719682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103894518-G-C

77719722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103894552-G-A

http://identifiers.org/hco/13/GRCh38#77719772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103894605-C-A

77719772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103894605-C-T

77719777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103894610-A-T

77719790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103894627-G-A

77719790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103894627-G-T

77720103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103894919-C-G

77720220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103895314-G-A

77720220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103895314-G-C

77720311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103895406-T-C

77720442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103895536-G-A

77720713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103895786-G-A

http://identifiers.org/hco/13/GRCh38#77720758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103895832-A-C

77720782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103895863-G-A

77720911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103895978-G-A

77720911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103895978-G-C

77721499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103896143-A-G

77721706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103896331-T-G

77721747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103896372-C-T

http://identifiers.org/hco/13/GRCh38#77721909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103896521-C-A

77721991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103896574-G-A

77721991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103896574-G-C

77722011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103896584-C-T

77722143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103896694-G-A

77722308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103896863-G-A

77722406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103897018-C-T

77722529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103897117-T-C

77722608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103897201-A-G

77722616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103897209-A-G

77722749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103897293-C-G

77722749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103897293-C-T

77722751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103897295-A-T

http://identifiers.org/hco/13/GRCh38#77723441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103897855-A-C

77723445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103897859-A-G

77723609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103897975-G-A

77723646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103898013-T-A

77723758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103898155-T-C

http://identifiers.org/hco/13/GRCh38#77723956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103898350-C-A

77724016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103898371-G-A

77724377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103898615-C-T

77724477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103898935-C-G

http://identifiers.org/hco/13/GRCh38#77724692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103899107-A-C

77724736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103899151-G-A

77727071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103900183-A-G

77727105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103900212-T-C

77727228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103900314-C-T

77727252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103900334-C-T

77727272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103900344-G-C

77727347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103900401-G-A

77727415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103900469-T-A

http://identifiers.org/hco/13/GRCh38#77727451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103900502-A-C

77727451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103900502-A-G

http://identifiers.org/hco/13/GRCh38#77727499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103900548-C-A

http://identifiers.org/hco/13/GRCh38#77727872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103900887-C-A

77727945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103900962-T-C

http://identifiers.org/hco/13/GRCh38#77728032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103901052-A-C

77728152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103901200-G-A

77728519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103901788-G-A

77728707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103901940-T-C

77728751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103901985-C-T

77729779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103903848-C-T

77730065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103904220-T-A

77730065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103904220-T-C

77730174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103904346-G-T

77730245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103904405-T-C

http://identifiers.org/hco/13/GRCh38#77731573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103904527-A-C

77731618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103904576-T-G

77731947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103904689-C-T

77731990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103904728-G-T

77731996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103904734-G-A

77732136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103904854-C-T

77732138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103904856-A-G

77732143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103904861-T-C

77732186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103904904-A-T

77732407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103905113-A-G

77732409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103905115-G-T

77732414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103905120-C-T

77732513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103905182-C-T

77732532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103905205-G-A

77733035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103905417-C-T

77733324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103905686-A-G

77733467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103905811-T-C

77733572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103905888-C-T

77733693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103905997-C-T

77734181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103906451-C-T

77734226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103906496-G-A

77734372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103906640-G-C

77735086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103907502-C-T

77735129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103907549-T-A

77735204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103907627-G-A

77735207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103907630-C-T

77735328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103907748-C-G

77736915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103916583-T-A

77736936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103916601-A-G

77737045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103916685-G-T

77737104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103916725-A-T

77737110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103916731-A-G

77737230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103916826-C-G

77737246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103916843-C-T

77737336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103916927-G-T

77737525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103917062-C-T

77737594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103917131-C-T

77737599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103917136-C-T

77737729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103917258-A-G

77737793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103917308-A-G

http://identifiers.org/hco/13/GRCh38#77737876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103917402-A-C

77737878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103917404-A-T

77737995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103917527-G-A

77738047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103917572-G-A

77738427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103917919-T-C

77738776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103918213-G-A

77738779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103918216-C-T

77738831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103918255-G-A

77738953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103918363-A-G

77739114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103918509-C-T

77739390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103918884-T-C

http://identifiers.org/hco/13/GRCh38#77739540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103919124-A-C

77739811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103919414-C-T

77739812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103919415-G-A

77739812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103919415-G-T

77739864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103919460-A-G

77739883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103919469-T-C

77740804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103919996-C-T

77740882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103920080-C-G

77740976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103920178-A-G

77740999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103920199-C-T

77741169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103920367-C-T

77741352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103920557-C-G

http://identifiers.org/hco/13/GRCh38#77741415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103920590-C-A

77741415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103920590-C-T

77741442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 103920618-T-G

http://identifiers.org/hco/13/GRCh38#77741501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103920675-C-A

77741501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103920675-C-T

77741577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103920741-T-G

77741610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103920773-A-G

77741610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103920773-A-T

77741681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103920844-T-G

77741686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103920849-A-T

77741756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103920891-T-C

77742519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103921194-G-A

77742775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103921437-G-T

77743074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103921728-T-C

77743237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103921890-T-C

77743242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103921895-T-C

77743273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103921924-G-A

77743273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103921924-G-T

http://identifiers.org/hco/13/GRCh38#77743388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103922030-C-A

77743388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103922030-C-G

77743436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103922108-T-A

77743446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103922118-T-A

77743484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103922297-T-A

77743484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103922297-T-G

77743583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103922394-A-G

77743608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103922422-A-G

77743608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103922422-A-T

77743628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103922442-C-T

77743737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103922569-T-G

77743749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103922578-A-G

77743840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103922661-G-A

77744156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103922992-G-A

77744156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103922992-G-T

77744202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103923029-G-T

77744246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103923073-T-C

77744247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103923074-G-A

77744247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103923074-G-T

77744491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103923307-G-A

77744491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103923307-G-T

77744537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103923352-T-G

77744585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103923399-T-C

77744680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103923599-G-A

77744937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103924041-G-A

http://identifiers.org/hco/13/GRCh38#77745112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103924178-A-C

77745112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103924178-A-G

77745145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103924206-C-T

77745305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103924350-C-G

77745618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103924627-A-G

77745926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103924933-A-G

77746139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103925148-T-C

77746385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103925415-A-T

77746401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103925429-A-G

77746572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103925556-G-A

77746638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103925622-T-C

77746638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103925622-T-G

77746850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, missense_variant
orthologous variants: 103925834-A-G

http://identifiers.org/hco/13/GRCh38#77746961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103925913-C-A

77746961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103925913-C-G

77746972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103925924-G-A

77747353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103926033-T-C

77747358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103926038-G-C

77747507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103926223-A-G

77747600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103926293-A-G

77747601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103926294-T-A

77747646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103926333-C-G

77747978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103926638-A-G

77748029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103926689-A-G

77748093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103926748-A-G

77748516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103927122-C-T

77748706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103927290-A-G

77749105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103927715-T-C

77749299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103927956-T-C

77749502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103928368-T-C

77749502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103928368-T-G

http://identifiers.org/hco/13/GRCh38#77749507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103928373-C-A

http://identifiers.org/hco/13/GRCh38#77749673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103928536-C-A

http://identifiers.org/hco/13/GRCh38#77749817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103928668-C-A

77749862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103928712-C-T

77750114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103928957-T-C

77750298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103929140-A-G

77751215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103931104-T-C

77751220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103931121-T-A

http://identifiers.org/hco/13/GRCh38#77751379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103931270-A-C

77751428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103931290-G-A

77751521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103931383-T-G

77751562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103931420-G-A

77751562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103931420-G-T

77751679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103931544-A-G

77751714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103931579-T-C

77751873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103931852-A-G

77751877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, undefined
orthologous variants: 103931856-G-A

77751958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, undefined
orthologous variants: 103931913-A-G

77751967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron_variant, undefined
orthologous variants: 103931921-T-C

77752227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103932149-G-T

77752239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103932161-T-A

77752268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103932190-G-T

http://identifiers.org/hco/13/GRCh38#77752313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103932257-C-A

77752313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103932257-C-T

77753371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103932772-A-G

77753374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103932775-T-C

http://identifiers.org/hco/13/GRCh38#77753426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103932804-A-C

77753426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103932804-A-G

77753426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103932804-A-T

77753433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103932818-A-G

77753435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103932820-G-A

77753435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103932820-G-T

77753490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103932855-G-A

77753490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103932855-G-T

77753709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103933012-T-C

77753717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103933020-C-G

77753961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103933197-T-C

77754038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103933259-G-C

77754066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103933286-T-C

77754082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103933302-A-G

77754289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103933455-G-C

77754423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103933582-G-T

77756353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103937703-C-G

77756382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103937739-T-G

http://identifiers.org/hco/13/GRCh38#77760740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103939871-C-A

77760797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103939922-T-A

77761205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103940367-A-G

77761259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103940416-A-T

77761742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103940637-T-C

77762926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103941061-A-G

77763005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103941138-A-G

77763070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103941202-A-G

77763070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103941202-A-T

77763074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: 103941206-G-T

http://identifiers.org/hco/13/GRCh38#77763114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103941246-C-A

77763348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 3 prime UTR variant
orthologous variants: 103941470-G-A

77763348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 3 prime UTR variant
orthologous variants: 103941470-G-T

77763380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 3 prime UTR variant
orthologous variants: 103941501-T-A

77763427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 3 prime UTR variant
orthologous variants: 103941547-A-G

77763429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 3 prime UTR variant
orthologous variants: 103941549-G-A

77763429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 3 prime UTR variant
orthologous variants: 103941549-G-T

77763480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 3 prime UTR variant
orthologous variants: 103941599-G-C

http://identifiers.org/hco/13/GRCh38#77763483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103941602-C-A

77763483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 3 prime UTR variant
orthologous variants: 103941602-C-T

77763486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 3 prime UTR variant
orthologous variants: 103941605-G-T

77763514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 3 prime UTR variant
orthologous variants: 103941634-T-A

77763514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 3 prime UTR variant
orthologous variants: 103941634-T-C

77763856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 3 prime UTR variant
orthologous variants: 103941972-T-A

http://identifiers.org/hco/13/GRCh38#77763936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26387
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#103942052-C-A