http://identifiers.org/hco/1/GRCh38#108560158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108934896-A-C

108560158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5 prime UTR variant
orthologous variants: 108934896-A-G

108560158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5 prime UTR variant
orthologous variants: 108934896-A-T

108560171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 108934884-T-A

108560171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 108934884-T-C

108560171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 108934884-T-G

http://identifiers.org/hco/1/GRCh38#108560172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#108934883-C-A

108560172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 108934883-C-G

108560172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 108934883-C-T

http://identifiers.org/hco/1/GRCh38#108560302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108934762-C-A

108560302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5 prime UTR variant
orthologous variants: 108934762-C-G

108560302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5 prime UTR variant
orthologous variants: 108934762-C-T

http://identifiers.org/hco/1/GRCh38#108560427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108934637-C-A

108560427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5 prime UTR variant
orthologous variants: 108934637-C-G

108560427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 5 prime UTR variant
orthologous variants: 108934637-C-T

108560552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense variant
orthologous variants: 108934512-G-A

108560552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense variant
orthologous variants: 108934512-G-T

http://identifiers.org/hco/1/GRCh38#108560587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108934478-C-A

108560587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108934478-C-T

108560590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108934475-G-A

108560590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108934475-G-C

108560590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108934475-G-T

108560619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108934443-G-A

108560695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108934332-T-A

108560707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108934318-T-C

108560748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108934287-T-A

108560889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108934155-G-A

108560952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108934094-T-A

108561031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108934022-G-C

108561522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108933570-A-G

108561616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108933475-A-G

108561777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, undefined
orthologous variants: 108933218-T-C

108561906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, undefined
orthologous variants: 108933085-A-G

108562111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108932861-G-T

108562460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108932533-A-G

108562808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108932232-T-G

108562908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108932155-A-G

108563001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108932067-G-A

108563001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108932067-G-C

108563108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108931965-A-G

108563108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108931965-A-T

http://identifiers.org/hco/1/GRCh38#108563113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108931961-C-A

http://identifiers.org/hco/1/GRCh38#108563221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108931888-C-A

108563221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108931888-C-T

108563374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108931728-G-T

108564000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108930752-C-T

108564099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108930657-T-C

108564353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108930454-G-C

108564499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108930295-T-C

108564525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108930238-G-A

108564590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108930174-C-T

108564985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108929765-A-G

108565030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108929715-A-G

108565708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108929194-G-A

108566157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108928584-C-G

108566267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108928494-A-G

108566481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108928084-A-G

108566538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108928030-G-A

108566557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108928011-T-C

108566613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108927981-G-A

108566667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108927927-G-T

http://identifiers.org/hco/1/GRCh38#108566675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108927919-A-C

108566810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108927790-A-G

108566810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108927790-A-T

108568390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108927575-A-G

108568499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108927472-A-G

108568506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108927465-T-C

http://identifiers.org/hco/1/GRCh38#108568611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108927361-C-A

108568611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108927361-C-T

108568700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108927258-C-T

108568744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108927214-T-A

108568766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108927193-A-T

108568880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108927091-C-T

108571717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108926042-G-A

108571717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108926042-G-T

108571870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108925951-G-T

108571880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108925941-T-G

108571907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108925914-T-C

108586523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108923794-A-G

http://identifiers.org/hco/1/GRCh38#108586538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108923779-A-C

108586783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108922645-A-G

108586867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108922549-A-G

108586874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108922542-A-G

108587126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108922157-G-A

108587879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108921501-A-G

108588185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108921189-T-C

108588233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108921001-G-C

108588329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108920911-G-A

108588395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108920845-A-G

108588474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108920771-C-T

http://identifiers.org/hco/1/GRCh38#108588787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108920631-C-A

108588787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108920631-C-T

108589000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108920374-A-G

108589115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108920270-A-T

108589232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108920156-T-C

108589342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108920056-C-T

http://identifiers.org/hco/1/GRCh38#108589565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108919815-C-A

108589565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108919815-C-T

108589574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108919806-T-A

108589594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108919788-T-C

108589698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108919701-C-G

108590116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108919363-C-T

108590204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108919269-A-G

108590262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108919208-T-C

108590303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108919167-G-A

108590434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108919032-A-G

http://identifiers.org/hco/1/GRCh38#108590587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108918905-A-C

108590695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108918813-C-T

108590853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108918654-T-C

108591096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108918398-T-C

108591229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108918265-C-G

108592327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108917580-T-C

108594487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108915855-G-A

108594906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108915564-A-G

108594986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108915498-T-C

108595914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108915498-A-G

108595921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108915505-G-A

108595965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108915544-G-A

108596251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108914178-G-A

108596382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108914046-C-T

108596441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108913994-A-G

108596451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108913984-T-C

108596584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108913853-G-A

108597343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108913320-C-T

108597361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108913302-C-T

108597444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108913242-G-T

108597537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108913156-C-T

108597552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108913138-T-C

108597615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108913077-G-C

108597658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108913035-T-G

108597847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108912865-A-G

108597905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108912818-C-G

108597905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108912818-C-T

108597966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108912760-G-A

108599265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108912546-A-G

108600496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108910797-A-G

108600752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108910550-G-A

108600752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108910550-G-T

http://identifiers.org/hco/1/GRCh38#108600780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108910529-C-A

108601006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108910334-G-T

108605212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108905064-C-T

108605395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108904900-C-T

http://identifiers.org/hco/1/GRCh38#108605410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108904887-A-C

108605448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108904849-A-T

108605603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108904724-T-C

108605943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108904603-C-T

108606071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108904533-G-A

108606071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108904533-G-T

108606099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108904505-T-C

108606180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108904424-T-C

108606192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108904412-A-G

108606192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108904412-A-T

108606241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense variant
orthologous variants: 108904360-G-A

108606241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense variant
orthologous variants: 108904360-G-C

108606241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense variant
orthologous variants: 108904360-G-T

108606307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108904295-T-C

108606344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108904280-A-G

108606344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108904280-A-T

108606358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108904266-G-T

108606475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108903918-G-A

108607220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108903758-C-T

108607321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108903661-G-A

108607389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108903595-A-G

108607409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108903575-G-A

108607739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108903426-G-C

http://identifiers.org/hco/1/GRCh38#108607796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108903366-C-A

108607877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108903284-A-G

108608553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108902490-T-G

108608619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108902415-G-A

108608825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108902281-G-T

108610362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108901677-G-C

108610628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108901444-C-T

108611470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108900691-A-G

108611540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108900624-G-A

108611549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108900615-A-G

108611697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108900484-C-T

108611702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108900479-A-G

108612003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108900221-T-G

http://identifiers.org/hco/1/GRCh38#108612026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108900194-C-A

108612026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108900194-C-T

108612142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108900092-G-T

108612224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense variant
orthologous variants: 108900010-A-G

108612227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense variant
orthologous variants: 108900007-C-G

http://identifiers.org/hco/1/GRCh38#108612351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108899885-C-A

108612351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108899885-C-T

108612352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108899884-G-A

108612352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108899884-G-T

108612391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108899845-T-A

http://identifiers.org/hco/1/GRCh38#108612441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108899812-A-C

108612441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108899812-A-G

108612490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108899768-A-G

108612501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108899758-G-T

http://identifiers.org/hco/1/GRCh38#108612660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108899245-C-A

108612740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108899173-C-T

108612773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108899155-G-A

108612775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108899153-A-G

108612778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108899150-C-G

108612959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108898985-T-C

108613005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108898943-T-A

108613101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108898847-A-T

108613141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108898741-T-A

108613141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108898741-T-G

http://identifiers.org/hco/1/GRCh38#108613299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108898579-C-A

108613299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108898579-C-T

108613329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108898549-A-G

http://identifiers.org/hco/1/GRCh38#108614143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108897635-C-A

http://identifiers.org/hco/1/GRCh38#108614195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108897621-A-C

108614232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108897602-T-A

108614232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108897602-T-C

108614295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108897553-C-G

108614295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108897553-C-T

108614397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108897445-A-G

108614926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108896982-G-A

http://identifiers.org/hco/1/GRCh38#108615063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108896828-A-C

108615278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108896636-A-T

108615862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108896050-C-T

108615895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108896017-G-A

108615895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108896017-G-T

108615974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108895950-C-T

108616285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108895789-A-T

108616320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108895754-G-C

108616344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108895708-A-T

108616362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108895692-A-G

http://identifiers.org/hco/1/GRCh38#108616415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108895638-C-A

108616415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense variant
orthologous variants: 108895638-C-T

108616458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108895594-T-A

108616458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108895594-T-C

http://identifiers.org/hco/1/GRCh38#108616475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108895577-A-C

108616475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108895577-A-G

108616560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108895534-G-A

108616560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108895534-G-T

108616886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108895240-A-G

108617100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108895027-C-T

108617143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108894984-G-A

108617155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108894972-G-A

108621019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108894402-G-T

108621031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108894390-A-T

108621263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108894161-A-G

108621413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108894024-C-T

108621623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108893805-G-A

108621679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108893753-A-T

108621800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108893537-G-T

108621876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108893473-C-T

http://identifiers.org/hco/1/GRCh38#108624474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108892888-C-A

108624474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108892888-C-G

108624474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108892888-C-T

http://identifiers.org/hco/1/GRCh38#108624578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108892808-C-A

108624578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108892808-C-G

108624594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108892787-G-A

108624604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108892777-A-G

http://identifiers.org/hco/1/GRCh38#108624613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108892768-C-A

108624613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108892768-C-G

108624613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108892768-C-T

108624730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108892644-G-A

108624730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108892644-G-T

108624754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108892620-G-A

108624868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108892552-A-T

108624908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108892509-T-A

http://identifiers.org/hco/1/GRCh38#108625312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108892164-C-A

108625427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108892049-T-A

108625506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108891966-T-C

108625560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108891934-G-T

108625594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108891901-A-G

108625618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108891877-T-A

108625664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108891832-T-C

108625954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108891321-T-G

108626001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108891277-G-A

108626001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108891277-G-T

108626077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108891201-T-C

http://identifiers.org/hco/1/GRCh38#108626130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108890559-C-A

108626130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108890559-C-T

108626140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108890550-T-C

108626197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108890490-G-T

http://identifiers.org/hco/1/GRCh38#108626250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108890446-A-C

108626250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108890446-A-G

108626314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108890383-T-C

http://identifiers.org/hco/1/GRCh38#108626316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108890381-C-A

http://identifiers.org/hco/1/GRCh38#108626376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108890335-C-A

108626376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108890335-C-T

108626414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108890302-T-C

108626473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108890249-T-C

http://identifiers.org/hco/1/GRCh38#108626490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108890242-C-A

108626514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108890218-C-G

108626514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108890218-C-T

http://identifiers.org/hco/1/GRCh38#108626553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108890183-C-A

108626611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108890123-T-C

108626726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108890020-A-G

108626758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108889988-T-G

http://identifiers.org/hco/1/GRCh38#108626822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108889931-C-A

108626911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108889838-G-A

108626911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108889838-G-T

http://identifiers.org/hco/1/GRCh38#108627003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108889745-C-A

http://identifiers.org/hco/1/GRCh38#108627175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108889588-C-A

108627196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108889555-A-G

http://identifiers.org/hco/1/GRCh38#108627218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108889533-C-A

108627218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108889533-C-T

108627219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108889532-T-C

108627252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108889499-C-T

108627337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108889427-G-A

108627349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108889413-G-T

http://identifiers.org/hco/1/GRCh38#108627399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108889365-A-C

108627455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108889311-A-G

http://identifiers.org/hco/1/GRCh38#108627485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108889281-C-A

108627485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108889281-C-G

108627486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108889280-T-C

http://identifiers.org/hco/1/GRCh38#108627568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108889163-A-C

108627568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108889163-A-G

108627568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108889163-A-T

108627767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108888869-A-T

108627827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108888816-G-A

108627827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108888816-G-T

http://identifiers.org/hco/1/GRCh38#108627864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108888780-A-C

108627864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108888780-A-G

108627864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108888780-A-T

108627982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108888724-A-T

108628033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108888672-A-G

http://identifiers.org/hco/1/GRCh38#108628079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108888631-C-A

108628079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108888631-C-T

108628104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108888606-G-C

108628104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108888606-G-T

108628110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108888600-A-G

http://identifiers.org/hco/1/GRCh38#108628132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108888585-C-A

108628132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108888585-C-T

108628287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108888435-T-C

108628372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108887633-T-C

108628381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108887624-A-G

108628469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108887534-A-G

108628523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108887480-A-G

108628537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108887466-T-C

108628578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108887395-T-C

108628578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108887395-T-G

108628656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108887149-A-G

108628708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108887091-C-G

108628821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108886978-T-G

108628827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108886972-T-C

108628830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108886969-A-T

108628842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108886956-C-T

108628911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108886916-T-G

http://identifiers.org/hco/1/GRCh38#108629519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108886298-C-A

108629519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108886298-C-T

108629554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108886262-T-C

108633658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108885154-A-G

108633743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108885071-C-T

108633762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108885052-A-G

108633872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108884936-G-C

108634454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108884441-G-A

108634518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108884375-G-A

http://identifiers.org/hco/1/GRCh38#108635059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108882703-C-A

108635059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108882703-C-G

108635064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108882698-A-G

108635108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 108882656-G-A

108635148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108882616-T-A

108635203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882567-T-C

108635203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882567-T-G

http://identifiers.org/hco/1/GRCh38#108635250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108882501-C-A

108635250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882501-C-T

http://identifiers.org/hco/1/GRCh38#108635295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108882459-A-C

108635301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882453-A-G

108635413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882358-G-A

108635413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882358-G-T

108635420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882351-T-C

108635435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882336-C-T

108635449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882325-A-T

108635490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882284-G-A

108635490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882284-G-C

108635490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882284-G-T

108635491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882283-T-C

108635559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882217-A-G

108635697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108882043-A-G

http://identifiers.org/hco/1/GRCh38#108635796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108881947-C-A

108635871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108881874-A-G

108635877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108881868-A-G

108636038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108881723-T-C

108636047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108881715-C-T

108636094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108881666-G-C

108636094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108881666-G-T

108636197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108881571-T-C

108636247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108881521-C-T

http://identifiers.org/hco/1/GRCh38#108636361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108881418-A-C

http://identifiers.org/hco/1/GRCh38#108636381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108881398-C-A

108636694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108881117-A-G

108636716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108881106-T-G

108636865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108880968-A-T

108636957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108880878-C-T

108636961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108880874-G-A

108636974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108880861-C-T

108637029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108880804-C-G

108637029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108880804-C-T

http://identifiers.org/hco/1/GRCh38#108637123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108880719-C-A

108637123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108880719-C-T

108637145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108880695-T-A

108637310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108880283-G-C

http://identifiers.org/hco/1/GRCh38#108637421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108880176-C-A

108637574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108880028-A-T

http://identifiers.org/hco/1/GRCh38#108637682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108879960-C-A

108637788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108879862-G-A

108637788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108879862-G-T

http://identifiers.org/hco/1/GRCh38#108637795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108879854-C-A

108637870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108879792-G-A

108637870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108879792-G-T

108637875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108879787-T-C

http://identifiers.org/hco/1/GRCh38#108637949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108879718-A-C

http://identifiers.org/hco/1/GRCh38#108638393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108879263-C-A

108638394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108879262-A-G

108638423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108879233-T-A

108638446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108879210-C-T

108638473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108879183-T-C

http://identifiers.org/hco/1/GRCh38#108638703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108878962-C-A

108638920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108878811-T-A

108638921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108878810-T-A

108639001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108878738-T-G

108639039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108878668-G-A

http://identifiers.org/hco/1/GRCh38#108639042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108878665-C-A

108639042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108878665-C-G

http://identifiers.org/hco/1/GRCh38#108639044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108878663-C-A

108639044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108878663-C-T

108642679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108875664-A-G

108642742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108875617-T-C

108643715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108874797-T-A

108643759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108874762-A-G

http://identifiers.org/hco/1/GRCh38#108644045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108874515-C-A

108644045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108874515-C-T

108644277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108874294-G-A

108644277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108874294-G-T

108644293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: intron variant
orthologous variants: 108874279-C-T

108644779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3 prime UTR variant
orthologous variants: 108873819-G-T

http://identifiers.org/hco/1/GRCh38#108644781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108873817-C-A

http://identifiers.org/hco/1/GRCh38#108644822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108873796-A-C

108644822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3 prime UTR variant
orthologous variants: 108873796-A-G

http://identifiers.org/hco/1/GRCh38#108644823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108873795-C-A

108644823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3 prime UTR variant
orthologous variants: 108873795-C-G

108644823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3 prime UTR variant
orthologous variants: 108873795-C-T

108644876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27637
most severe consequence: 3 prime UTR variant
orthologous variants: 108873776-T-C