http://identifiers.org/hco/8/GRCh38#28023340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65885740-C-A

28023353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: synonymous variant
orthologous variants: 65885727-G-A

28023358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65885722-C-T

28023504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65885579-T-C

http://identifiers.org/hco/8/GRCh38#28023559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65885540-A-C

28023559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65885540-A-G

28023570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65885524-T-A

28024145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65884891-C-G

28024286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65884695-A-G

http://identifiers.org/hco/8/GRCh38#28024288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65884693-A-C

28024288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65884693-A-G

28024303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65884678-C-T

28024341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65884579-G-A

28024412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65884505-C-T

28024413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65884504-G-A

28024500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, undefined
orthologous variants: 65884417-A-T

28024533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65884387-C-T

28024586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65884335-C-T

28024925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65884001-C-T

28026016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65883564-A-T

28026024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65883556-C-T

28026030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65883550-A-G

28026225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65883365-T-C

28026225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65883365-T-G

28026320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65883263-T-C

28026337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65883241-C-T

28026359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65883214-T-C

28026445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65883153-C-G

28026453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65883145-A-G

28026983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65882526-C-T

28027065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65882444-G-T

28027081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65882428-G-C

28027081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65882428-G-T

http://identifiers.org/hco/8/GRCh38#28027109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65882401-C-A

28027109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65882401-C-T

28027112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65882398-A-T

http://identifiers.org/hco/8/GRCh38#28027140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65882370-C-A

28027140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65882370-C-T

http://identifiers.org/hco/8/GRCh38#28027156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65882354-C-A

28027287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65882218-A-G

28027312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65882191-G-C

28027312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65882191-G-T

28027521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65882041-T-C

28027667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65881881-A-G

28028422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65880581-A-G

28028528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65880487-G-A

28029035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65879715-A-G

28029099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65879653-A-T

http://identifiers.org/hco/8/GRCh38#28029218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65879487-C-A

28029218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65879487-C-T

http://identifiers.org/hco/8/GRCh38#28029221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65879484-C-A

28029221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65879484-C-G

28029221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65879484-C-T

28029248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65879459-G-A

28029248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65879459-G-T

28029318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65879389-C-T

28029325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65879382-C-T

http://identifiers.org/hco/8/GRCh38#28029403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: splice acceptor variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65879304-C-A

http://identifiers.org/hco/8/GRCh38#28029426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65879264-C-A

28029426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65879264-C-T

28029453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65879237-A-G

28029805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65879205-A-T

28029816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65879194-C-T

28029987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65879040-C-T

28030190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65878914-T-A

28030190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65878914-T-C

28030190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65878914-T-G

28030229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65878877-A-G

28030229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65878877-A-T

http://identifiers.org/hco/8/GRCh38#28030303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65878801-C-A

28030303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 65878801-C-G

28030303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 65878801-C-T

http://identifiers.org/hco/8/GRCh38#28030331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65878773-C-A

28030331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65878773-C-T

28030342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65878762-G-A

28030342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65878762-G-T

http://identifiers.org/hco/8/GRCh38#28030346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65878758-C-A

28030346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65878758-C-T

http://identifiers.org/hco/8/GRCh38#28030356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65878748-C-A

28030411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65878693-G-A

28030411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65878693-G-T

28030454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65878565-A-G

28030604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65878160-T-A

28030736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65878049-C-G

28030744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65878041-G-T

28030836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65877942-A-G

28030876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65877834-G-A

28031208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65877603-A-G

28031208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65877603-A-T

28031379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 65877432-G-A

28031379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 65877432-G-C

28031427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65877382-G-A

28031432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65877377-G-T

28031479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65877331-G-A

28031479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65877331-G-T

http://identifiers.org/hco/8/GRCh38#28031512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65877298-C-A

28031512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65877298-C-G

28031512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65877298-C-T

28031571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65877239-G-A

28031571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65877239-G-T

28031755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65877078-A-T

28032002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65876857-T-C

28033240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65876465-G-A

28033472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65876230-T-C

28033624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65876071-C-T

28033723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65875972-G-A

28033736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65875956-A-G

28033754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, undefined
orthologous variants: 65875938-T-G

28033803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65875883-G-A

28033803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65875883-G-T

http://identifiers.org/hco/8/GRCh38#28033812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65875874-C-A

http://identifiers.org/hco/8/GRCh38#28033816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65875870-A-C

http://identifiers.org/hco/8/GRCh38#28034425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65874934-A-C

28034425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65874934-A-G

28034893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65874498-C-T

28035068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65874345-G-A

28035069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65874344-G-A

28035325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65874121-T-C

28039649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65873888-A-T

28039883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65873679-A-G

28039987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65873582-T-C

28039991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65873531-C-T

http://identifiers.org/hco/8/GRCh38#28040151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65873365-C-A

28040151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65873365-C-G

28040151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65873365-C-T

http://identifiers.org/hco/8/GRCh38#28040391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65873154-A-C

28040449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65873080-G-C

28040513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65873028-C-T

http://identifiers.org/hco/8/GRCh38#28040600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65872945-A-C

28040600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65872945-A-T

28040620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65872929-G-C

28040620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65872929-G-T

28040922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65872733-G-T

28040932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65872723-G-A

28040932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65872723-G-T

http://identifiers.org/hco/8/GRCh38#28041002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65872656-C-A

28041002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65872656-C-T

28041070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65872595-A-T

28041071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65872594-T-C

http://identifiers.org/hco/8/GRCh38#28041073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65872592-C-A

28041073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65872592-C-G

28041073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65872592-C-T

http://identifiers.org/hco/8/GRCh38#28041076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65872589-C-A

28041076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65872589-C-G

28041076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65872589-C-T

28041120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65872545-C-G

28041207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: synonymous variant
orthologous variants: 65872458-G-A

28041207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65872458-G-C

http://identifiers.org/hco/8/GRCh38#28041229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65872437-C-A

28041229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65872437-C-T

http://identifiers.org/hco/8/GRCh38#28041271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65872420-C-A

28041285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65872406-T-C

28041420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65872275-C-T

28041778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65871795-C-T

28041780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65871793-A-G

28041781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65871792-A-G

28041790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65871783-C-T

http://identifiers.org/hco/8/GRCh38#28041809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65871761-A-C

28043254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65871498-G-A

28043529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65871230-A-G

http://identifiers.org/hco/8/GRCh38#28043691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65871079-A-C

28044041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65870760-G-T

28044944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65870055-A-T

28045010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65869990-G-A

28045036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65869964-A-T

28045138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65869009-A-T

http://identifiers.org/hco/8/GRCh38#28045440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65868716-A-C

28045440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65868716-A-G

28045480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65868693-T-C

28045499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65861629-G-T

28047417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65860802-G-A

28047417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65860802-G-T

28047521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65860699-G-A

28047521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65860699-G-C

28047521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65860699-G-T

http://identifiers.org/hco/8/GRCh38#28047531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65860689-C-A

28047531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 65860689-C-T

28053789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: -A-G

28054009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: -C-T

28055849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65857219-A-G

http://identifiers.org/hco/8/GRCh38#28055892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65857176-C-A

28055892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65857176-C-G

28055941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65857127-A-G

28055941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65857127-A-T

http://identifiers.org/hco/8/GRCh38#28055953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65857116-C-A

28055953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65857116-C-G

http://identifiers.org/hco/8/GRCh38#28055987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65857082-C-A

28056036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5_prime_UTR_variant, intron_variant, stop_gained, synonymous_variant
orthologous variants: 65857033-G-A

28056036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65857033-G-C

28056036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 65857033-G-T

28056075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65856995-G-T

28056081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65856989-T-C

http://identifiers.org/hco/8/GRCh38#28056093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65856977-C-A

28056093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65856977-C-T

28056111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65856959-G-A

28056111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65856959-G-C

28056111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65856959-G-T

http://identifiers.org/hco/8/GRCh38#28058321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65856476-A-C

28058321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65856476-A-G

28058321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65856476-A-T

http://identifiers.org/hco/8/GRCh38#28058420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65856363-C-A

http://identifiers.org/hco/8/GRCh38#28058429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65856354-C-A

28058429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65856354-C-G

28058490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65856294-C-T

28059041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65856110-G-A

28059077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65856069-G-C

28059176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65855970-T-C

http://identifiers.org/hco/8/GRCh38#28060249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65855373-C-A

28060278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65855344-G-A

28060278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65855344-G-C

28060278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65855344-G-T

28060515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 65855125-C-G

28060515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 65855125-C-T

28060543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65855097-C-G

28060582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65855058-A-G

28060667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65854974-C-T

28060730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65854908-T-G

28060794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65854863-C-T

28060812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65854845-C-T

28060994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65854671-A-T

28061257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, undefined
orthologous variants: 65854510-G-A

28061268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, undefined
orthologous variants: 65854499-T-C

28061355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, undefined
orthologous variants: 65854414-C-T

28061367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, undefined
orthologous variants: 65854402-T-C

28061748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65853926-G-A

28061748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65853926-G-C

28062102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65853435-T-C

28062807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65853045-A-G

28062882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852972-G-C

28062985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852888-T-A

28063012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852867-G-A

28063082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852800-T-A

28063082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852800-T-C

28063104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852777-G-C

28063104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852777-G-T

28063172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852714-G-T

28063191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, undefined
orthologous variants: 65852695-G-T

28063261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852624-C-G

http://identifiers.org/hco/8/GRCh38#28063304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65852584-A-C

http://identifiers.org/hco/8/GRCh38#28063363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65852525-C-A

28063398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852497-G-A

28063630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852293-G-T

28063683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852245-A-G

28063698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852232-A-G

28063827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852157-C-G

28063827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852157-C-T

28063836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65852145-G-T

28064076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65851957-C-G

28064076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65851957-C-T

28064472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65851099-G-T

28064534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: synonymous variant
orthologous variants: 65851038-C-T

http://identifiers.org/hco/8/GRCh38#28064694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65850878-C-A

28064694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65850878-C-T

28064858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65850707-T-A

28064858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65850707-T-C

28064881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65850684-G-C

28065497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65849923-T-C

28065566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65849835-G-A

http://identifiers.org/hco/8/GRCh38#28065603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65849799-C-A

28065658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65849745-T-G

28066839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65849543-A-G

28066912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65849487-G-A

http://identifiers.org/hco/8/GRCh38#28067203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65849194-C-A

28067372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65848965-G-C

28067372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65848965-G-T

28067411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65848925-A-G

28067414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65848922-T-C

28067441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65848875-T-C

28067478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65848842-A-T

28067591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65848732-T-C

28067666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65848657-A-G

28067686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65848637-C-G

28067806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65848506-G-A

28067806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65848506-G-T

http://identifiers.org/hco/8/GRCh38#28067820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65848492-C-A

28067820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65848492-C-T

28067831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65848481-G-T

http://identifiers.org/hco/8/GRCh38#28067833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65848479-C-A

28067833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65848479-C-T

28067868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65848448-T-A

28067868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65848448-T-C

28067868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65848448-T-G

28068186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65847506-G-A

28068186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65847506-G-T

28068220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65847476-T-C

http://identifiers.org/hco/8/GRCh38#28068330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65847366-C-A

28068330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: synonymous variant
orthologous variants: 65847366-C-T

28068334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65847362-A-G

28068334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65847362-A-T

28068394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65847302-A-G

http://identifiers.org/hco/8/GRCh38#28068535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65847174-C-A

28068535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65847174-C-T

28068538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65847171-G-A

28068538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65847171-G-T

28068542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65847167-C-T

28068580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65847138-G-A

28068580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65847138-G-T

28068606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65847112-G-T

28068614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65847104-C-G

28069402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65846487-T-C

http://identifiers.org/hco/8/GRCh38#28069430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65846440-C-A

28069430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65846440-C-G

28069430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65846440-C-T

28069539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65846350-C-T

http://identifiers.org/hco/8/GRCh38#28069681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65846207-A-C

28069724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 65846167-T-C

28069744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65846147-A-G

28069873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65846028-A-G

28069873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65846028-A-T

28069932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65845975-T-C

28069934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65845973-C-T

28070004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, undefined
orthologous variants: 65845930-C-T

http://identifiers.org/hco/8/GRCh38#28070019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65845921-C-A

28070226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65845727-T-G

http://identifiers.org/hco/8/GRCh38#28070298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65845644-C-A

28070298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: synonymous variant
orthologous variants: 65845644-C-T

28070312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: missense variant
orthologous variants: 65845630-A-G

http://identifiers.org/hco/8/GRCh38#28070368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65845574-C-A

28070368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65845574-C-T

28070389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65845555-G-A

28070500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65845462-T-C

28070504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65845458-T-A

28070504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65845458-T-C

28070667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65845294-C-T

28070703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65845247-C-G

28070703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65845247-C-T

28070845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65845054-A-G

28071356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65844591-C-T

28071456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65844531-G-T

28072021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65843996-C-G

28072073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65843923-C-T

28072144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, undefined
orthologous variants: 65843852-A-G

28072158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65843837-A-T

28072551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, undefined
orthologous variants: 65843479-T-A

28072738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65843310-G-A

28072738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65843310-G-T

http://identifiers.org/hco/8/GRCh38#28073397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65843096-C-A

28073397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65843096-C-T

http://identifiers.org/hco/8/GRCh38#28074312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65842521-C-A

28074419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5 prime UTR variant
orthologous variants: 65842423-A-G

http://identifiers.org/hco/8/GRCh38#28074513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65842332-C-A

28074513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65842332-C-T

28075194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65841789-C-T

http://identifiers.org/hco/8/GRCh38#28075432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65841538-C-A

28075545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65841435-C-T

28075785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65841156-G-T

28075888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65841052-C-T

28075952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65840991-G-A

http://identifiers.org/hco/8/GRCh38#28077004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65840589-C-A

28077004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65840589-C-T

28077850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65839308-A-G

http://identifiers.org/hco/8/GRCh38#28078108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65839013-A-C

28078296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65838831-A-G

28078531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65838678-T-C

28078557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65838648-C-T

28078871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65838421-G-A

28078960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65838330-G-A

28078966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65838324-C-T

28079079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65838212-C-G

28079176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron_variant, undefined
orthologous variants: 65838120-A-G

28082147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65837910-G-A

28082416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65837687-G-A

28082461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65837659-T-A

28082461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65837659-T-C

28082537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65837572-T-C

http://identifiers.org/hco/8/GRCh38#28082677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65837361-A-C

28082690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65837343-G-A

28082772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65837197-A-G

28082772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65837197-A-T

28083009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65836801-G-C

http://identifiers.org/hco/8/GRCh38#28083023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65836787-A-C

28083130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65836690-G-A

28083135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65836685-C-T

28083239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65836593-T-C

28083384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65836450-A-G

28083427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65836407-C-T

28083604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65836231-T-C

28083605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: intron variant
orthologous variants: 65836230-G-A

28083793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5 prime UTR variant
orthologous variants: 65836065-A-G

28083813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 65836022-G-A

28083813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 65836022-G-C

28083813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 65836022-G-T

http://identifiers.org/hco/8/GRCh38#28083847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65835998-C-A

28083847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5 prime UTR variant
orthologous variants: 65835998-C-T

28083871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5 prime UTR variant
orthologous variants: 65835968-T-C

28083928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33550
most severe consequence: 5 prime UTR variant
orthologous variants: 65835909-A-G