124619679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132314236-T-C

124619695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132314247-A-G

http://identifiers.org/hco/10/GRCh38#124619764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132314321-C-A

124620032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132314507-G-A

124620037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132314512-T-G

124620117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132314595-A-G

124620197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132314673-C-T

124620206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132314681-G-A

124620318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132314807-G-T

124620380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132314862-T-C

124620416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132314875-G-C

124620416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132314875-G-T

http://identifiers.org/hco/10/GRCh38#124620511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132314922-C-A

124620550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132314924-G-A

124620550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132314924-G-T

124620551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132314925-G-T

124620662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132315043-G-A

124620662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132315043-G-T

124620848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132315235-A-G

124620865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132315252-G-A

124620865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132315252-G-T

124620907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132315294-G-T

124620948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132315339-T-C

124621116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132315490-G-T

http://identifiers.org/hco/10/GRCh38#124621506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132315801-C-A

124621506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132315801-C-T

http://identifiers.org/hco/10/GRCh38#124621930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132316171-A-C

124621930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132316171-A-T

124621944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132316184-G-C

124621991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132316220-G-C

124621991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132316220-G-T

124622032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132316249-A-G

124622139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132316335-G-A

124622139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132316335-G-T

124622169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132316368-G-T

124622172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132316371-T-C

http://identifiers.org/hco/10/GRCh38#124622496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132316740-C-A

124622496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132316740-C-T

124622590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132316829-G-A

124622590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132316829-G-T

124622807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132317020-G-A

124622838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132317040-G-A

124622838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132317040-G-C

124622838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132317040-G-T

124622962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132317131-G-T

124622963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: 132317132-A-T

http://identifiers.org/hco/10/GRCh38#124623164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132317321-C-A

124623327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: missense variant
orthologous variants: 132317457-G-A

124623383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: synonymous_variant, undefined
orthologous variants: 132317513-C-T

http://identifiers.org/hco/10/GRCh38#124623646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132317775-C-A

124623646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132317775-C-T

124623679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132317817-G-A

124623679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132317817-G-T

http://identifiers.org/hco/10/GRCh38#124623702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132317849-C-A

124623702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132317849-C-T

http://identifiers.org/hco/10/GRCh38#124623842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132317923-C-A

124623842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132317923-C-T

124623896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132317977-A-G

124624190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132318943-T-C

124624255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132319012-G-A

124624357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132319126-A-T

124624377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132319146-C-T

124624858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132319451-C-G

124624862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132319455-C-T

124625074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132319579-C-T

124625102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132319608-A-G

124625214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132319718-A-G

124625689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132320174-T-G

http://identifiers.org/hco/10/GRCh38#124625817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132320252-C-A

124625817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132320252-C-T

124626072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132320464-G-A

124626095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132320472-G-A

124626102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132320479-G-A

124626102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132320479-G-C

124626166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132320529-C-T

124626176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132320539-C-T

124626177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132320540-T-C

124626506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132320857-A-T

124626618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132320974-T-C

124626694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132321044-C-T

124626799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132321115-G-A

124627097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132321445-A-G

124627294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132321637-G-T

124627348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132321673-G-A

http://identifiers.org/hco/10/GRCh38#124627498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132321792-C-A

124627503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132321797-C-T

124627684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132321934-G-A

124627856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132322062-G-A

124627856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132322062-G-C

124627856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132322062-G-T

124628171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132322383-C-T

124628248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132322439-G-A

124628248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132322439-G-C

http://identifiers.org/hco/10/GRCh38#124628408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132322584-C-A

124628408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132322584-C-G

124628448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132322601-G-A

http://identifiers.org/hco/10/GRCh38#124628454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132322607-A-C

124628499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132322653-T-C

124628668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132322804-G-A

124628668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132322804-G-C

124628686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132322823-T-C

124628938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132323055-T-C

http://identifiers.org/hco/10/GRCh38#124629534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132324278-C-A

124630138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132324370-C-T

124630139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132324371-G-A

124630141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132324374-G-A

124630141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132324374-G-T

124630188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132324420-G-A

124630539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132324870-G-A

124630562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132324892-A-G

124631056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132325323-G-A

124631169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132325434-G-T

http://identifiers.org/hco/10/GRCh38#124631437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132325664-A-C

http://identifiers.org/hco/10/GRCh38#124631746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132325902-C-A

http://identifiers.org/hco/10/GRCh38#124631829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132325977-A-C

124632455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132326659-C-T

124632511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132326709-A-G

124632624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132326836-G-A

124637477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132330351-G-A

124637477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132330351-G-C

124637583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132330464-A-T

124637833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132330737-A-G

124637899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132330787-G-A

124637982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132330837-G-A

124638268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132330955-G-C

124638268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132330955-G-T

124638300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132330974-G-A

124638303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132330977-G-C

124638826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132331364-C-T

124638907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132331444-G-T

124639093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132331623-T-C

124639130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132331668-C-T

124639163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132331706-G-A

124639319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132331819-C-T

124639378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132331886-G-A

124639380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132331888-G-A

124639492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132331993-G-A

124642707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132332668-A-G

124642747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132332695-T-C

124643002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132332920-G-A

124643016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132332934-G-A

124643130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132333037-G-A

124643412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132333295-G-A

124643521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132333404-G-A

124644388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132334201-C-T

124644911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132334664-T-C

124645001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132334736-C-T

124645140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132334916-G-A

124645140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132334916-G-C

124645140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132334916-G-T

124645650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132335412-C-T

124645680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132335443-G-A

124645881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132335643-G-A

124645881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132335643-G-T

124645963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132335711-T-C

124645974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132335722-C-G

124645974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132335722-C-T

124646124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132335858-C-T

124646220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132335933-A-G

124647619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132336830-A-G

124647636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132336847-G-C

124647739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132336918-C-T

124647918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132337064-C-T

124648148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132337317-T-G

124648153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132337322-A-G

124648390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132337551-C-T

http://identifiers.org/hco/10/GRCh38#124648489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132337640-C-A

124648489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132337640-C-G

124648489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132337640-C-T

http://identifiers.org/hco/10/GRCh38#124648529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132337676-C-A

124648619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132337743-T-C

124649052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132338125-C-G

124649215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132338288-C-T

124649407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132338408-T-C

124649418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132338419-C-G

124649484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132338460-C-T

124649724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132338626-C-T

124649737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132338639-A-G

124649880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132338714-T-C

124650088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132338954-A-G

http://identifiers.org/hco/10/GRCh38#124650642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132339622-C-A

124651096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132339989-G-A

124651151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132340048-C-T

124654935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132340411-G-C

124654951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132340429-G-A

124654999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132340478-C-T

http://identifiers.org/hco/10/GRCh38#124655130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132340600-A-C

124655203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132340641-G-A

124655259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132340695-C-T

124655346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132340784-C-T

124655482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132340875-C-T

http://identifiers.org/hco/10/GRCh38#124656011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132341370-C-A

124656119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132341456-C-T

124656135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132341470-G-A

124656135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132341470-G-C

124656222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132341554-G-A

124656222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132341554-G-C

124656288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132341606-G-A

124656375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132341682-C-G

124656543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132341810-G-A

124656556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132341823-G-A

124656575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132341842-G-C

124656803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342002-C-G

124656894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342033-T-G

124657014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342098-T-C

124657056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342127-A-G

http://identifiers.org/hco/10/GRCh38#124657139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132342306-C-A

124657139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342306-C-T

124657140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342307-A-G

124657177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342347-C-T

124657196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342380-G-T

124657236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342414-G-A

124657430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342598-G-A

124657567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342726-T-C

http://identifiers.org/hco/10/GRCh38#124657568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132342727-A-C

124657568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342727-A-G

http://identifiers.org/hco/10/GRCh38#124657600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132342762-C-A

124657600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342762-C-G

124657693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342894-C-T

124657787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132342967-C-T

124657868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132343049-C-T

124657938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132343109-G-A

124657993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132343163-C-T

124657996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132343166-T-C

124658125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132343287-C-T

124658256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132343404-C-G

124658256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132343404-C-T

124659068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132343879-T-C

124659123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132344021-G-C

http://identifiers.org/hco/10/GRCh38#124659173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132344109-A-C

124659244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132344186-T-C

124659444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132344327-T-G

124659483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132344367-T-C

124659612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132344477-G-A

124660178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132344726-G-A

124660178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132344726-G-C

124660194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132344742-T-C

124660420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132344932-C-T

http://identifiers.org/hco/10/GRCh38#124660737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132345212-A-C

124661706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132347576-T-C

124661720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132347590-C-G

124661890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132347749-C-T

124661951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132347808-G-A

124663158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132348520-T-C

124663659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132348988-G-A

124663814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349156-T-G

http://identifiers.org/hco/10/GRCh38#124663871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132349242-C-A

http://identifiers.org/hco/10/GRCh38#124663908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132349276-C-A

124663912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349280-C-G

124663912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349280-C-T

124664164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349504-T-A

124664164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349504-T-C

124671050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349879-G-A

124671050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349879-G-C

124671064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349899-T-C

124671083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349918-G-A

124671083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349918-G-T

124671091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349927-G-C

124671091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349927-G-T

124671125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349955-G-A

124671125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349955-G-T

124671148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349975-C-T

124671149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132349976-C-T

124671249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132350064-G-A

124671249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132350064-G-T

124671787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132350504-C-T

124671956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132350662-G-A

124672019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132350725-C-G

124672019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132350725-C-T

124672062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132350766-T-C

124672092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132350793-G-A

124672185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132350877-G-A

124672227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132350917-T-C

124672280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132351108-G-A

124672379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132351250-C-T

124672437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132351305-G-A

124672501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132351366-G-A

124672501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132351366-G-C

http://identifiers.org/hco/10/GRCh38#124672520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132351385-C-A

124672620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132351494-A-G

124672675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132351555-G-A

124672911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132351720-A-G

124674854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132353439-A-G

124675011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132353585-C-T

124675045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132353618-C-T

124675053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132353627-G-T

124675110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132353695-C-G

124675870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132354925-T-C

124675881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132354936-G-A

124675899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132354957-G-A

124676029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132355058-G-A

124676272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132355240-C-T

124676348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132355315-G-A

124677345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132356283-C-T

124677419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132356356-G-A

124677566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132356476-A-T

124677678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132356585-G-T

124677989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132356894-G-A

124678874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132358231-C-T

124678960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132358310-C-T

http://identifiers.org/hco/10/GRCh38#124679410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132358713-C-A

124679410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132358713-C-T

124679489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132359017-G-A

124679538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132359073-G-A

124679805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132359339-C-T

124679874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132359407-G-A

124679874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132359407-G-C

124680083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132359614-G-A

124680108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132359636-A-G

124680184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132359710-T-A

124680367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132359867-T-C

124680409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132359902-C-T

http://identifiers.org/hco/10/GRCh38#124680468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132359956-C-A

124680801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132360345-G-A

124681026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132360607-C-T

124681220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132360752-T-A

124681390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132360893-T-A

http://identifiers.org/hco/10/GRCh38#124681553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132361057-C-A

124681553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132361057-C-G

124681553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132361057-C-T

124681567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132361066-A-G

http://identifiers.org/hco/10/GRCh38#124681664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132361175-C-A

124681679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: synonymous variant
orthologous variants: 132361190-G-A

124681787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: synonymous variant
orthologous variants: 132361298-A-G

http://identifiers.org/hco/10/GRCh38#124681889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132361400-A-C

http://identifiers.org/hco/10/GRCh38#124681947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132361458-C-A

124681947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: missense variant
orthologous variants: 132361458-C-G

124681947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: missense variant
orthologous variants: 132361458-C-T

124681956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: missense variant
orthologous variants: 132361467-A-G

124682126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: synonymous variant
orthologous variants: 132361637-T-A

124682126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: synonymous variant
orthologous variants: 132361637-T-C

124682165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: synonymous variant
orthologous variants: 132361676-T-C

124683162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132362549-T-C

124683217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132362604-T-C

124683248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132362635-T-C

124683914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132363289-C-G

124684094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132363415-G-C

124684201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132363524-C-T

124684308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132363609-C-T

124685044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132364553-G-A

124685100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132364606-T-C

124685173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132364669-G-A

124685266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132364756-T-C

124685580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132365049-T-C

124686782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132365286-G-C

124687192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132365671-T-C

124687301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132365769-A-G

124687579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132366039-G-A

124687616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132366080-T-A

124687679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132366152-A-G

124687716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132366190-A-T

124689251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132367253-T-A

124689281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132367274-A-G

124689373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132367398-C-T

124689876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132367944-C-T

124689948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132368007-G-A

http://identifiers.org/hco/10/GRCh38#124690256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132368279-C-A

124690256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132368279-C-T

124690295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132368315-T-G

124690383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132368392-G-A

124690735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132368697-T-A

124690959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132368896-A-G

124691085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132369009-T-C

124691091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132369015-C-T

124691712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132369638-G-A

http://identifiers.org/hco/10/GRCh38#124691851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132369832-C-A

124692253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132370143-C-T

124692641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132370342-G-A

124692811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132370399-A-G

124693544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132370772-G-A

124693606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132370834-G-A

124693749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132370959-G-A

124693819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132371015-G-A

124693820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132371016-T-C

124694099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132371361-T-C

http://identifiers.org/hco/10/GRCh38#124694300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132371504-C-A

124694709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132372035-C-G

124694760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132372073-A-G

124694841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132372139-G-T

124694857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132372155-C-T

124694894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132372193-G-A

124694934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132372225-G-A

124695062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132372339-T-A

124695062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132372339-T-C

124695199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132372469-T-C

124695205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132372475-A-G

124695317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132372534-T-C

124695617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132372786-A-G

http://identifiers.org/hco/10/GRCh38#124695644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132372814-C-A

124695648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132372818-C-T

124695904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132373056-G-A

124695964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132373133-A-T

http://identifiers.org/hco/10/GRCh38#124696038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132373197-C-A

124696043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132373202-G-T

124696046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132373205-T-C

http://identifiers.org/hco/10/GRCh38#124696067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132373221-C-A

124696067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132373221-C-T

http://identifiers.org/hco/10/GRCh38#124696258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132373399-C-A

124696258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132373399-C-T

http://identifiers.org/hco/10/GRCh38#124696374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132373508-C-A

124696374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132373508-C-T

124696466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132373594-G-A

124696722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132373773-G-A

124697430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132374403-C-T

124697826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132374796-T-A

124697873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132374827-T-A

124697915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132374869-C-T

124698056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132375011-G-A

124698281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132375197-T-C

124698289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132375209-G-A

124698289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132375209-G-C

124698289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132375209-G-T

124700137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132375919-G-A

124700196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132375977-C-T

124700299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376082-C-T

124700309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376090-A-G

124700321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376102-C-T

124700409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376179-C-T

124700450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376219-A-G

124700498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376266-C-T

124700564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376316-C-T

124700603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376354-G-A

124700766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376512-T-C

124700984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376725-G-C

124701082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376811-T-C

124701100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376829-G-T

124701223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376921-G-A

124701223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376921-G-C

124701261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132376959-A-G

124701422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132377080-C-T

124701618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132377266-T-C

124701622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132377270-G-C

124701748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132377395-C-T

http://identifiers.org/hco/10/GRCh38#124701834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132377479-A-C

124701883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132377518-G-A

124701903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132377543-G-A

124701910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132377562-G-T

124702188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132377908-C-T

http://identifiers.org/hco/10/GRCh38#124702197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132377916-C-A

124702416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132378088-T-G

124703626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132378468-C-T

124703680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132378517-G-T

http://identifiers.org/hco/10/GRCh38#124703724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132378529-C-A

124703724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132378529-C-G

124703724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132378529-C-T

124703731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132378536-A-G

124703967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132378723-G-A

http://identifiers.org/hco/10/GRCh38#124704027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132378782-C-A

124704027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132378782-C-T

124704030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132378785-G-T

http://identifiers.org/hco/10/GRCh38#124704068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132378821-C-A

124704068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132378821-C-T

124704194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132378925-A-G

124704367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132379133-A-G

124704537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132379296-T-A

124704537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132379296-T-C

124704537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132379296-T-G

124704718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132379412-T-C

124704718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132379412-T-G

124704819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132379483-G-A

http://identifiers.org/hco/10/GRCh38#124705422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132379951-C-A

124705422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132379951-C-G

124705446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132379975-T-C

124705509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380031-T-C

124705523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380044-A-T

http://identifiers.org/hco/10/GRCh38#124705577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132380094-C-A

124705577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380094-C-T

http://identifiers.org/hco/10/GRCh38#124705583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132380100-C-A

http://identifiers.org/hco/10/GRCh38#124705652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132380170-C-A

124705652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380170-C-T

124705653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380171-T-C

http://identifiers.org/hco/10/GRCh38#124705662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132380180-C-A

124705690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380206-G-A

124705690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380206-G-C

124705690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380206-G-T

124705733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380251-C-T

http://identifiers.org/hco/10/GRCh38#124705765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132380275-C-A

124705770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380280-T-A

124705770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380280-T-C

124705784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380294-T-C

http://identifiers.org/hco/10/GRCh38#124705812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132380323-C-A

124705812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380323-C-T

124705826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380336-T-C

124706226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380483-G-A

http://identifiers.org/hco/10/GRCh38#124706318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132380585-A-C

124706379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380632-G-A

124706379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380632-G-C

124706523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132380754-T-A

124706628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 132380857-G-A

124706741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 132380970-T-A

124706769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 132380998-T-C

http://identifiers.org/hco/10/GRCh38#124706827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132381065-C-A

124706827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 132381065-C-T

124706884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 132381111-C-T

124706921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132381148-G-A

124706921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132381148-G-C

124706921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132381148-G-T

http://identifiers.org/hco/10/GRCh38#124706992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132381200-C-A

124707010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132381218-G-A

124707010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132381218-G-T

124707310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132381552-C-T

124707311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132381553-G-A

124707359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132381576-G-C

http://identifiers.org/hco/10/GRCh38#124707447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132381662-C-A

http://identifiers.org/hco/10/GRCh38#124707904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132381763-C-A

124707904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132381763-C-T

124708045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132381896-G-A

124708045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132381896-G-T

124708073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132381925-T-C

124708209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132382055-T-C

124708217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132382063-T-A

124708304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132382148-T-C

124708304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132382148-T-G

124708503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132382368-C-T

124708826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132382669-T-G

124708841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132382684-G-C

124709029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132382854-C-T

124709130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132382942-C-T

124709371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132383146-T-G

124709485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132383263-G-A

124709485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132383263-G-C

124710301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132383678-T-C

124710322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132383699-C-T

124710371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132383746-A-G

124710626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132383970-C-T

124710627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132383971-G-A

124713433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132385597-G-A

http://identifiers.org/hco/10/GRCh38#124713488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132385651-C-A

http://identifiers.org/hco/10/GRCh38#124713495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132385658-C-A

124713501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132385663-C-T

124713569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132385730-A-G

http://identifiers.org/hco/10/GRCh38#124713790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132385974-C-A

http://identifiers.org/hco/10/GRCh38#124713833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132386015-C-A

124713961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132386129-G-A

124714059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132386205-T-C

124714100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132386255-G-T

124714256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132386365-T-A

124714342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132386436-G-T

http://identifiers.org/hco/10/GRCh38#124714758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#132386907-C-A

124715238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132387274-T-C

124715274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132387310-G-T

124715301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132387334-G-A

124715370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132387376-G-A

124715469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132387458-A-G

124715484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132387473-G-C

124715853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132387800-G-A

124715859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132387806-C-T

124715869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132387816-C-T

124716273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132388144-A-G

http://identifiers.org/hco/10/GRCh38#124716358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132388203-A-C

124716650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132388472-T-C

124716768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132388565-C-G

124716768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132388565-C-T

124716820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132388606-A-G

124716822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132388608-A-G

124716842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132388628-T-C

http://identifiers.org/hco/10/GRCh38#124716864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132388645-A-C

124716866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132388647-T-C

124716970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132388748-G-C

124717084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132388867-T-C

124717096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132388879-G-A

124717239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132389012-G-A

124717273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132389038-T-G

124717593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132389189-G-A

124717671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132389221-G-A

124717837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132389288-G-C

124717869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132389323-T-A

124717943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132389411-A-G

124718168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132389612-C-T

124719194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132390252-A-G

124719209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132390262-C-T

124719606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132390636-C-G

124719606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132390636-C-T

124719622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132390652-G-A

124719649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132390689-G-A

124719658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132390698-T-G

124720665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132391294-C-G

124720665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132391294-C-T

124720793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132391418-A-G

124722740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132393476-C-T

124722803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132393557-G-C

124722810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132393564-G-A

124723283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132394091-G-A

124723502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132394288-A-G

124723660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132394432-T-G

124723762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132394515-G-A

124723923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132394623-C-T

124724300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132394961-T-C

http://identifiers.org/hco/10/GRCh38#124724536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132395128-A-C

124724715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132395284-C-G

124724741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132395309-G-C

124724793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132395359-G-A

124725043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132395620-G-A

124725946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132396457-A-G

124726014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132396494-G-C

124726106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132396551-A-T

http://identifiers.org/hco/10/GRCh38#124726363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132396756-C-A

124726469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132396863-G-A

124726577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132396980-C-T

124726581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132396981-T-C

124726673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132397102-C-T

124726914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132397622-C-G

124726914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132397622-C-T

124727318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132397744-C-G

124727897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132398295-T-C

124728098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132399578-T-C

124728100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132399580-G-A

124728108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132399590-T-C

http://identifiers.org/hco/10/GRCh38#124728178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132399660-C-A

http://identifiers.org/hco/10/GRCh38#124728413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132399844-A-C

124728603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132399996-C-T

124728609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132400002-G-A

124728895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132400290-T-C

124729013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132400350-G-A

124729057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132400368-G-A

124729184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132400489-T-C

124729196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132400501-C-G

124729239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132400522-C-T

124729392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132400669-T-C

124729461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132400741-G-C

124729461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132400741-G-T

124729729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132400903-A-G

124729801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132400969-T-C

124729929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132401080-T-C

http://identifiers.org/hco/10/GRCh38#124730130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132401232-C-A

124730193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132401289-T-C

124730248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132401345-A-G

124730350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132401467-G-A

124730374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132401491-G-C

124730384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132401501-G-A

124730498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132401601-T-G

124730785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132401853-A-G

http://identifiers.org/hco/10/GRCh38#124730829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132401895-C-A

124730829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132401895-C-T

124730831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132401897-T-C

124730842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132401908-G-A

124731085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132402349-A-G

124731512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132402923-T-G

124731698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132403326-A-G

124731746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132403386-T-C

http://identifiers.org/hco/10/GRCh38#124732173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132403777-C-A

124732185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132403788-G-A

124732292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132403886-A-G

124732409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132404019-G-C

124732455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132404062-C-T

124732974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132404275-G-A

124733301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132404553-G-A

124733301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132404553-G-C

124733358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132404612-G-A

124733399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132404653-T-C

124733414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132404668-C-G

124733599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132404827-T-C

124733662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132404893-T-C

124733878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132405360-C-T

124734125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132405613-G-A

124734191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132405677-A-G

http://identifiers.org/hco/10/GRCh38#124734669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132405943-C-A

124734878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132406625-C-T

124734940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132406693-T-C

124734963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132406728-G-A

http://identifiers.org/hco/10/GRCh38#124734978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132406746-C-A

124734988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132406756-T-A

124735308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132407062-C-T

124735352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132407100-G-A

124735490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132407244-T-C

http://identifiers.org/hco/10/GRCh38#124735555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132407278-C-A

124735813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132407435-G-T

124735842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132407462-C-T

124735986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132407597-T-G

124736138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132407731-G-C

124736367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132407984-C-G

124736533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132408150-G-A

124736577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132408194-G-A

124736969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132408419-A-G

http://identifiers.org/hco/10/GRCh38#124737053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132408476-A-C

124737123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132408530-C-T

124737228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132408629-C-T

124737366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132408719-A-G

124737500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132408944-T-C

124737647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132409068-C-T

124737807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132409185-G-C

124738322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132409660-G-A

124738373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132409715-T-C

124738373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132409715-T-G

http://identifiers.org/hco/10/GRCh38#124738553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132409925-C-A

124738628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132409993-C-T

124738633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132409996-C-T

124738796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132410155-G-A

124738987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132410388-T-C

http://identifiers.org/hco/10/GRCh38#124739011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132410408-C-A

http://identifiers.org/hco/10/GRCh38#124739057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132410452-C-A

http://identifiers.org/hco/10/GRCh38#124739060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132410455-A-C

http://identifiers.org/hco/10/GRCh38#124739064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132410457-C-A

http://identifiers.org/hco/10/GRCh38#124739352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132410747-A-C

124739449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132410829-T-C

124739452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132410832-G-A

124739514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132410894-A-G

124739549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132410929-C-G

124739549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132410929-C-T

124739564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132410944-T-C

124739963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132411352-A-G

124740303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132411680-A-G

http://identifiers.org/hco/10/GRCh38#124740627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132412006-C-A

http://identifiers.org/hco/10/GRCh38#124740781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132412145-C-A

124740781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132412145-C-T

124741024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132412392-C-T

124741090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132412467-T-C

124741246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132412617-G-A

124742150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132413540-T-A

124742291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132413656-T-C

124742334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132413696-T-A

124742334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132413696-T-C

124742402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132413767-G-A

124742516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132413883-C-T

124742597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132413962-A-G

124742624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132413990-T-C

124743139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132414477-C-G

124743464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132414807-C-T

http://identifiers.org/hco/10/GRCh38#124743643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132414958-A-C

124743805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron variant
orthologous variants: 132415123-G-A

124743893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: intron_variant, undefined
orthologous variants: 132415200-G-T

124744038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5 prime UTR variant
orthologous variants: 132415325-C-T

124744117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5 prime UTR variant
orthologous variants: 132415396-T-C

124744117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5 prime UTR variant
orthologous variants: 132415396-T-G

124744143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5 prime UTR variant
orthologous variants: 132415423-C-T

124744307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5 prime UTR variant
orthologous variants: 132415584-C-T

124744309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5 prime UTR variant
orthologous variants: 132415586-G-A

124744309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28968
most severe consequence: 5 prime UTR variant
orthologous variants: 132415586-G-T