10439892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38825826-G-C

10440042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38825977-C-T

10440263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38826190-T-A

10440282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38826211-G-A

http://identifiers.org/hco/4/GRCh38#10440490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38826425-C-A

10440602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38826536-A-G

10440763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38826697-C-G

10440763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38826697-C-T

10441035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38826904-A-G

10441076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38826948-C-T

10441431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827305-T-C

10441436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827309-T-A

10441436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827309-T-G

10441486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827347-C-T

10441741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827528-T-C

10441770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827560-T-C

10441771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827561-G-A

10441771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827561-G-C

10441833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827596-T-G

10441867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827628-G-T

10441952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827707-T-C

10442174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827901-G-A

10442174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827901-G-T

http://identifiers.org/hco/4/GRCh38#10442179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38827906-C-A

10442179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827906-C-T

10442192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827917-G-T

10442219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38827945-T-C

10442336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38828067-T-C

10442618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38828314-A-G

http://identifiers.org/hco/4/GRCh38#10442648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38828345-C-A

10442677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38828371-A-G

10442760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38828447-G-T

http://identifiers.org/hco/4/GRCh38#10442923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38828587-C-A

10442940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38828604-A-G

http://identifiers.org/hco/4/GRCh38#10442965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38828627-C-A

10442965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38828627-C-T

http://identifiers.org/hco/4/GRCh38#10443036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38828683-A-C

10443036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38828683-A-G

10443036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 3 prime UTR variant
orthologous variants: 38828683-A-T

10443194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38828845-A-G

10443236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38828887-A-G

10443591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38829245-T-A

10443691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38829345-G-A

http://identifiers.org/hco/4/GRCh38#10443775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38829432-C-A

10443818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38829475-T-C

10443972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38829629-T-A

10443972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38829629-T-C

10444099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38829756-T-C

10444100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38829757-T-C

10444135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38829792-C-G

10444224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38829893-G-A

10444232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38829901-A-G

10444250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38829919-C-T

10444367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38830036-G-A

10444388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38830057-G-A

10444388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38830057-G-T

10444424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38830093-T-C

10444427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38830096-T-C

10444450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38830119-T-C

10444453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38830122-T-C

10444460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38830129-C-T

10444757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38830429-T-A

10444866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38830535-G-C

10444867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38830536-A-T

10444871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38830540-T-C

10445000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38830666-T-C

10445093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38830759-A-G

http://identifiers.org/hco/4/GRCh38#10445159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38830825-A-C

10445159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38830825-A-G

10445159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38830825-A-T

10445255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38830921-C-T

10445288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38830954-C-G

10445288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38830954-C-T

10445438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38831104-C-G

10445438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38831104-C-T

10445531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38831197-A-T

10445552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38831218-T-C

10445552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38831218-T-G

10445858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38831524-G-A

10445888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38831554-C-G

10445888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38831554-C-T

10445912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: missense variant
orthologous variants: 38831578-T-A

10445912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38831578-T-C

10445975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38831638-T-A

10445975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38831638-T-G

10446029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38831692-A-G

10446224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: synonymous variant
orthologous variants: 38831890-T-G

10446349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5 prime UTR variant
orthologous variants: 38832011-G-A

10446349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5 prime UTR variant
orthologous variants: 38832011-G-C

http://identifiers.org/hco/4/GRCh38#10446377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38832039-C-A

10446377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5 prime UTR variant
orthologous variants: 38832039-C-G

10446420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5 prime UTR variant
orthologous variants: 38832080-T-C

10446426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5 prime UTR variant
orthologous variants: 38832086-G-A

10446426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5 prime UTR variant
orthologous variants: 38832086-G-C

http://identifiers.org/hco/4/GRCh38#10446475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38832138-C-A

10446475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5 prime UTR variant
orthologous variants: 38832138-C-T

10446488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5 prime UTR variant
orthologous variants: 38832152-T-C

10446520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5 prime UTR variant
orthologous variants: 38832181-C-G

http://identifiers.org/hco/4/GRCh38#10446663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38832321-C-A

10446663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38832321-C-G

10446663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38832321-C-T

10446667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38832327-T-A

10446667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38832327-T-C

10446673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38832333-A-G

10446726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38832384-C-T

10446812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38832461-G-A

10446825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38832474-C-T

10446857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38832505-C-T

10446872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38832525-T-C

10447084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38832708-T-A

10447084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38832708-T-C

10447271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38833041-A-G

10447301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38833096-C-T

10447312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38833106-G-T

10447375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38833159-G-C

http://identifiers.org/hco/4/GRCh38#10447625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38833298-A-C

10447625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38833298-A-G

10447999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38833532-G-A

http://identifiers.org/hco/4/GRCh38#10448075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38833607-C-A

http://identifiers.org/hco/4/GRCh38#10448106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38833651-C-A

10448382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38833855-C-T

10448611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38834035-A-T

10448789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38834188-A-G

10448806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38834202-G-T

10448864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38834263-T-G

10449041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38834441-C-G

10449113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38834502-G-A

10449148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38834537-T-A

10449158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38834547-T-C

10449164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38834553-T-A

10449176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38834560-G-C

10449517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38834747-A-G

http://identifiers.org/hco/4/GRCh38#10449728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38834977-A-C

10449748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38834997-T-C

http://identifiers.org/hco/4/GRCh38#10449765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38835014-A-C

10449765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38835014-A-G

10449772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38835022-C-T

10449773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38835023-C-T

http://identifiers.org/hco/4/GRCh38#10449799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38835055-A-C

10449812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38835068-G-A

10449923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38835128-C-G

http://identifiers.org/hco/4/GRCh38#10449954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38835159-A-C

10449954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38835159-A-G

10450024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38835208-T-C

10450058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38835242-T-A

10450247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron variant
orthologous variants: 38835764-C-T

10450360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38835849-A-G

10450462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38836131-C-T

10450466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38836136-A-G

http://identifiers.org/hco/4/GRCh38#10450742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38836385-C-A

10450841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38836464-G-C

10450856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38836479-G-A

10451002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38836606-T-A

10451188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837004-C-G

10451260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837069-G-T

10451288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837094-G-T

10451363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837150-T-C

10451374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837172-G-C

10451422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837217-T-C

10451729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837491-T-C

10451835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837582-G-A

10451861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837607-T-C

10451868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837614-G-T

http://identifiers.org/hco/4/GRCh38#10451874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38837620-C-A

http://identifiers.org/hco/4/GRCh38#10451961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38837696-C-A

10451961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837696-C-G

10451961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837696-C-T

http://identifiers.org/hco/4/GRCh38#10451963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38837698-C-A

http://identifiers.org/hco/4/GRCh38#10452091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38837754-C-A

10452091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837754-C-T

10452146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837821-G-A

10452146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837821-G-T

10452152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837828-G-T

http://identifiers.org/hco/4/GRCh38#10452153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38837829-C-A

10452153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837829-C-T

10452252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38837913-T-C

10452551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38838045-T-C

10452734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38838154-G-A

10452752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38838172-G-T

10452866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38838279-C-T

10452873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38838287-T-C

10452890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38838304-T-C

10452969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38838363-C-G

http://identifiers.org/hco/4/GRCh38#10452972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38838366-C-A

10452972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38838366-C-T

http://identifiers.org/hco/4/GRCh38#10453074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38838452-C-A

http://identifiers.org/hco/4/GRCh38#10453202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38838561-A-C

10453293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38838626-G-A

10453299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38838632-C-T

10453421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38838698-T-C

http://identifiers.org/hco/4/GRCh38#10453457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38838726-C-A

10453537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38838808-G-A

http://identifiers.org/hco/4/GRCh38#10453603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38838879-C-A

10453772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839078-A-G

10453846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839149-G-A

10453846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839149-G-T

http://identifiers.org/hco/4/GRCh38#10453875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38839179-C-A

10453875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839179-C-T

10453877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839181-G-A

10453889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839187-T-C

http://identifiers.org/hco/4/GRCh38#10453965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38839226-C-A

10453965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839226-C-T

10454002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839266-G-C

10454015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839287-T-A

10454015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839287-T-C

10454052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839323-C-G

10454052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839323-C-T

10454067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839330-G-T

10454071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839334-G-A

http://identifiers.org/hco/4/GRCh38#10454079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38839342-C-A

10454105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839361-T-G

10454336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839553-G-A

10454410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839625-G-A

10454528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839731-A-G

10454570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839773-T-C

http://identifiers.org/hco/4/GRCh38#10454636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38839838-C-A

10454708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38839911-T-A

10454708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38839911-T-C

10454708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38839911-T-G

10454958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38840100-T-A

10454958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38840100-T-C

10454959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38840101-G-A

10455035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38840170-G-A

10455035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38840170-G-T

10455065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38840204-G-A

10455065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38840204-G-T

http://identifiers.org/hco/4/GRCh38#10455075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38840220-C-A

10455083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38840228-T-C

10455198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38840322-T-C

http://identifiers.org/hco/4/GRCh38#10455327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#38840440-A-C

10455362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38840479-G-T

10455793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38840856-A-G

10455802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38840868-C-T

10455815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38840881-A-T

10455908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38840959-T-A

10455951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38841002-G-C

10455996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38841047-G-A

10456070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38841116-C-T

10456202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38841247-T-C

10456440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841493-C-T

10456987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38841890-G-A

10456987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38841890-G-T

http://identifiers.org/hco/4/GRCh38#10457020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38841920-A-C

10457405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38842125-C-T

10457509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842209-G-A

http://identifiers.org/hco/4/GRCh38#10457539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38842236-C-A

10457539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842236-C-T

10457596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38842288-G-A

10457596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38842288-G-T

10457672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842346-A-G

10457895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842543-G-A

10457936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842571-T-C

10457954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842589-C-T

10458032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842662-G-A

http://identifiers.org/hco/4/GRCh38#10458081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38842718-C-A

10458237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842964-G-A

10458237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842964-G-C

10458379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38843094-T-C

10458511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38843222-G-A

10458536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38843247-T-G

10458750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38843883-T-C

http://identifiers.org/hco/4/GRCh38#10459160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#38844256-A-C

10459170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844326-G-T

10459176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844452-T-C

10459181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844457-G-C

10459410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38844701-T-G

10459791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38845063-G-A

10459835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38845110-C-T