2663692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32884927-T-A

2663730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32884968-G-A

2663780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32885007-C-G

2663791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32885016-T-C

2664022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32885214-A-G

2664037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32885230-G-T

http://identifiers.org/hco/6/GRCh38#2664207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32885377-C-A

2664301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32885483-T-A

2664437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32885764-G-A

2664437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32885764-G-T

2664505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32885831-G-A

2664869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32886156-G-T

2665154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32886402-G-T

2665191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32886410-G-A

http://identifiers.org/hco/6/GRCh38#2665226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32886445-C-A

2665299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32886506-G-A

2665300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32886507-C-T

2665302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32886509-G-A

2665302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32886509-G-T

2665324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32886531-G-T

2665329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32886536-T-G

2665443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32886650-T-G

http://identifiers.org/hco/6/GRCh38#2665467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32886670-C-A

2665502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32886704-A-T

2665508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32886710-A-G

2665605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32886813-T-C

2665849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32887035-A-G

2665849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32887035-A-T

2665851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32887040-G-A

2665851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32887040-G-C

2665946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32887149-A-T

2666912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32888195-G-A

2666912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32888195-G-T

2667121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32888399-G-A

2667121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32888399-G-T

2667216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32888483-G-T

2667454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32888788-C-T

http://identifiers.org/hco/6/GRCh38#2667488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32888822-C-A

2667495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32888829-C-G

2667521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32888855-G-A

2667722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32889034-A-T

2667766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32889078-C-T

2667808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32889108-T-C

2667841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 3 prime UTR variant
orthologous variants: 32889140-T-G

2668314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32889659-G-A

2668508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32890049-A-T

2668665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32890206-G-A

2669161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32890668-G-A

2669580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32891070-A-T

2669640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32891140-G-C

2669685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32891185-C-T

2669777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32891259-G-A

2669787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32891269-T-C

2669891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32891365-G-A

2670742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32892296-C-G

2670917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32892437-T-A

http://identifiers.org/hco/6/GRCh38#2671159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32892651-C-A

2671159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32892651-C-T

2671160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32892652-G-A

2671160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32892652-G-T

http://identifiers.org/hco/6/GRCh38#2671207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32892698-C-A

2671207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32892698-C-T

2671221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32892710-T-C

2671385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32892968-C-T

2671427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32893005-C-T

http://identifiers.org/hco/6/GRCh38#2671448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32893026-A-C

2671644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32893206-C-T

2671682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32893240-C-T

2672106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32893845-G-T

2672117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32893873-G-A

2672152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32893973-G-A

2672157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32893978-C-G

2672534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32894310-C-T

2672618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32894393-A-G

2672731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32894846-A-G

2672731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32894846-A-T

http://identifiers.org/hco/6/GRCh38#2672860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32894931-C-A

2672956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32895026-T-C

2673044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32895097-C-T

2673097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32895155-T-C

2673630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32895681-C-T

2673762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32895811-G-T

2674140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32896174-G-A

2674334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32896364-C-G

http://identifiers.org/hco/6/GRCh38#2674919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32896623-C-A

2674919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32896623-C-G

2674957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32896660-T-C

2675024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32896721-G-A

2675024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32896721-G-T

2675155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32896848-G-T

2675165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32896858-G-A

2675165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32896858-G-T

2675300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32896980-C-T

2675413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32897090-C-T

2675458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32897135-T-C

2676411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32897952-A-T

2676748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32898268-A-G

2676902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32898410-G-A

http://identifiers.org/hco/6/GRCh38#2677027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32898533-C-A

2677350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899115-G-A

http://identifiers.org/hco/6/GRCh38#2677489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32899249-C-A

2677489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899249-C-G

2677629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899371-A-G

2677665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899393-G-A

2677668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899396-C-T

2677720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899451-G-A

2677720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899451-G-C

2677779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899499-G-A

2677779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899499-G-C

2677801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899515-G-A

2677801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899515-G-T

2678130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899757-G-A

2678130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899757-G-C

2678130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899757-G-T

2678131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899758-T-A

2678131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899758-T-C

2678139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899766-T-A

2678139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899766-T-C

2678160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32899786-G-A

2678273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: synonymous variant
orthologous variants: 32899895-G-A

2678406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32900031-T-A

2678406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32900031-T-C

2678446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32900070-G-A

2678446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32900070-G-C

2678446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32900070-G-T

2678472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32900096-G-T

2678519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32900138-T-A

2678519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32900138-T-C

2679201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32900562-G-A

2679201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32900562-G-C

2679201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32900562-G-T

2679448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32900807-A-T

http://identifiers.org/hco/6/GRCh38#2679503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32900873-C-A

2679503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32900873-C-T

2679557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32900916-G-A

http://identifiers.org/hco/6/GRCh38#2679569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32900927-C-A

2679569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32900927-C-G

http://identifiers.org/hco/6/GRCh38#2679620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32900978-C-A

2679703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32901057-A-G

2679906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32901228-T-A

2680023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32901337-T-C

2680081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32901395-A-G

2680081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32901395-A-T

2680124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32901438-A-T

2680126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32901440-G-C

2680126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32901440-G-T

2680176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32901488-A-G

http://identifiers.org/hco/6/GRCh38#2680733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32902050-C-A

2680832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32902151-G-A

2680956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32902275-T-C

2680958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32902277-G-A

2681330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32902650-T-C

2681544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32902874-T-C

http://identifiers.org/hco/6/GRCh38#2681789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32903097-C-A

2682324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32903631-G-T

2682379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32903680-G-A

2682728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32903975-G-A

2682728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32903975-G-T

http://identifiers.org/hco/6/GRCh38#2682928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32904339-C-A

2682928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904339-C-T

2682959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904370-C-G

2682961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904372-G-A

2682962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904373-G-A

2682962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904373-G-T

2683096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32904518-G-A

2683132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32904554-G-A

http://identifiers.org/hco/6/GRCh38#2683203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32904621-C-A

2683203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904621-C-G

2683268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904685-G-A

2683268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904685-G-T

2683341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904720-T-C

2683344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904723-A-G

2683393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904735-G-T

2683413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904755-G-A

2683413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904755-G-T

2683438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904780-G-A

2683438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904780-G-T

2683439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904781-A-T

2683594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904828-A-G

2683724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904926-G-A

2683773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32904974-G-A

2683831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32905027-C-T

2685016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32905706-G-A

2685142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32905828-C-G

2685613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32906269-G-A

2685613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32906269-G-T

http://identifiers.org/hco/6/GRCh38#2685647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32906305-C-A

2685647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32906305-C-T

2685661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32906319-T-A

2685661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32906319-T-G

2685701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32906349-G-T

2686902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32907679-G-A

2686929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32907706-C-T

2686949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32907724-C-T

2686950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32907725-G-A

2686960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32907735-A-G

2686991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32907766-C-T

2688876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32908787-C-T

2689000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32908909-G-A

2689000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32908909-G-T

http://identifiers.org/hco/6/GRCh38#2689021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32908931-C-A

http://identifiers.org/hco/6/GRCh38#2689047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32908957-A-C

2689360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909347-T-A

2689497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909488-C-T

2689542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909532-A-G

2689819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909980-A-T

2689968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32910163-G-A

http://identifiers.org/hco/6/GRCh38#2690111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32910794-C-A

http://identifiers.org/hco/6/GRCh38#2690466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32911137-C-A

2690555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911226-T-G

2690571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911244-G-T

2690665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911307-C-T

2691227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911475-C-T

2691333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911559-A-T

2691433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911634-T-C

2691858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32912196-A-G

2692154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32912470-A-G

2692423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32912733-A-T

2692454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32912761-T-C

2692507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32912812-A-G

2692604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32912917-G-T

2692632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32912944-A-G

2692632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32912944-A-T

2692660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32912952-T-C

2692660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32912952-T-G

http://identifiers.org/hco/6/GRCh38#2692672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32912965-C-A

2692672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32912965-C-G

2692672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32912965-C-T

2692719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913009-A-G

http://identifiers.org/hco/6/GRCh38#2692838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32913113-C-A

2692838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32913113-C-T

2692924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913202-C-G

2692934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913210-G-C

2692934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913210-G-T

2692942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913218-T-G

2692968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913234-G-A

2692968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913234-G-C

2692968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913234-G-T

2693024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913299-C-T

2693032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913307-C-G

http://identifiers.org/hco/6/GRCh38#2693143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32913582-C-A

2693143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913582-C-T

2693335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913777-G-A

2693338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913780-G-A

2693477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913914-T-G

2693549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913978-C-T

2693585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914014-A-G

http://identifiers.org/hco/6/GRCh38#2693660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32914073-C-A

2693800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914168-C-T

2694460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914483-A-G

2694506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914511-G-A

2694506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914511-G-C

2694506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914511-G-T

2694523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914528-G-A

2694523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914528-G-C

2694523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914528-G-T

2694581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914534-G-A

2694581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914534-G-C

2694581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914534-G-T

2694582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914535-T-C

2694582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914535-T-G

2694584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914537-G-A

2694584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914537-G-C

2694586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914539-G-A

2694586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914539-G-C

2694587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914540-G-A

2694587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914540-G-C

2694587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914540-G-T

2694714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914655-T-C

http://identifiers.org/hco/6/GRCh38#2694948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32914839-C-A

2695331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32915214-T-C

2695380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32915259-G-A

2695580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32915411-A-T

2695581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32915412-T-C

2695730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32915560-G-A

2695869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32915677-C-T

http://identifiers.org/hco/6/GRCh38#2695918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32915725-A-C

2695951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32915752-A-T

2695962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32915762-A-G

2696021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32915810-G-A

http://identifiers.org/hco/6/GRCh38#2696042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32915831-A-C

2697514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32916128-G-A

2697600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32916206-G-C

2697833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32916520-C-T

2698555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32917859-G-A

2698555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32917859-G-T

2698747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32918247-C-T

2698781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32918280-C-T

2699075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32918560-T-C

http://identifiers.org/hco/6/GRCh38#2699101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32918584-C-A

2699809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32919096-A-G

2700864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32920983-A-G

2701024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921137-T-C

2701205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921315-G-A

2701387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921490-G-A

2701387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921490-G-C

2701450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921548-C-T

http://identifiers.org/hco/6/GRCh38#2701461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32921559-C-A

2701640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921966-C-T

2701644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921970-G-A

2701761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32922096-G-A

2701943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32922381-C-T

2701946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32922384-C-G

2701951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32922389-C-T

2702070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32922504-T-G

2702167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32922619-A-G

2702257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32922705-G-A

2702257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32922705-G-C

2704586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32923386-C-T

2704766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32923569-C-G

2704794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32923597-G-C

2705185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32924013-T-G

2705186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32924014-T-G

2705252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32924076-A-G

2706309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32924262-T-G

2706553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32924486-A-T

2706571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32925021-G-A

2707093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32925485-G-A

2707095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32925487-G-A

2707105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32925497-G-A

2707210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32925597-A-G

2707325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32925722-G-A

2707334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32925731-G-C

2707431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32925830-A-G

2707470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32925869-C-T

2707795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32926202-T-C

2708133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32926539-T-C

2708133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32926539-T-G

2708286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32927069-G-A

http://identifiers.org/hco/6/GRCh38#2708457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32927238-A-C

2708921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32927675-T-C

2709072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32927759-G-A

2709311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32928280-A-G

2711456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32928985-A-T

2711641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32929170-C-T

2711646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32929175-T-A

2711646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32929175-T-G

2711649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32929178-C-G

2711896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32929400-A-G

http://identifiers.org/hco/6/GRCh38#2712278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32929763-A-C

2712278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32929763-A-G

2712371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32929854-G-A

2712384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32929867-G-T

2712415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32929898-T-G

2712729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32931191-A-G

2712892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32931330-C-G

2713395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32932304-A-G

http://identifiers.org/hco/6/GRCh38#2713418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32932326-C-A

2713515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32932420-C-G

2713668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32932575-T-A

2713720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32932627-T-C

2713836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32932743-G-A

2714062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32932951-T-A

2714062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32932951-T-C

2716648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32934034-T-G

http://identifiers.org/hco/6/GRCh38#2716700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32934094-A-C

2716713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32934107-G-C

2716944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32934311-G-A

2717161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32934479-T-G

2717547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32934849-A-G

2717669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32934973-A-G

2718276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32935512-T-C

2718864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32936039-G-A

2719405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32936608-A-G

2719414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32936616-G-A

2719497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32936700-A-G

2719606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32936811-G-T

2719832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32936959-T-C

http://identifiers.org/hco/6/GRCh38#2721945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32937898-A-C

2722512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32938437-A-T

2722532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32938457-T-G

http://identifiers.org/hco/6/GRCh38#2722622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32938563-C-A

http://identifiers.org/hco/6/GRCh38#2722651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32938592-C-A

http://identifiers.org/hco/6/GRCh38#2722780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32938716-A-C

2722820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32938756-T-C

2722915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32938831-A-T

2723313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32939154-G-A

http://identifiers.org/hco/6/GRCh38#2723506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32939347-C-A

2723506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32939347-C-G

2723506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32939347-C-T

2723590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32939413-T-C

http://identifiers.org/hco/6/GRCh38#2724198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32939712-A-C

2724342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32939851-G-C

2724347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32939856-G-T

2724693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32940516-G-A

2724693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32940516-G-T

http://identifiers.org/hco/6/GRCh38#2724717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32940553-C-A

2724807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32940634-C-T

2724808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32940635-G-A

2724808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32940635-G-T

2724812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32940639-T-C

2724816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32940643-T-C

2725731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32940736-G-A

2725750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32940753-G-A

2725750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32940753-G-C

http://identifiers.org/hco/6/GRCh38#2725757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32940760-C-A

http://identifiers.org/hco/6/GRCh38#2725859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32940855-C-A

2725948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32940945-C-T

2725994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32940986-G-A

2726070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32941054-C-T

2726205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32941207-C-T

2726216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32941218-C-T

2726256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32941257-G-A

2727240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32941917-C-G

2727429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32942108-T-C

http://identifiers.org/hco/6/GRCh38#2727567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32942482-C-A

2728280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32942884-T-A

2728304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32942905-C-T

2728529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32943120-T-C

2728597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32943189-G-A

2728657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32943237-C-T

2728732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32943322-T-C

2729006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32943588-C-T

2730250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32944263-G-A

http://identifiers.org/hco/6/GRCh38#2730290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32944303-C-A

2730443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32944459-G-T

2730468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32944488-C-T

2730558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32944572-A-G

2730714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32944730-G-A

2730759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32944775-A-G

2731072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32945087-G-T

2731369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32945354-G-A

2731477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32945464-C-T

2731521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32945509-G-A

2731595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32945571-C-T

2731647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32945621-A-G

2731899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32946355-G-A

2731981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32946416-A-G

http://identifiers.org/hco/6/GRCh38#2732142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32946645-C-A

2732142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32946645-C-T

2732143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32946646-G-A

2732143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32946646-G-C

http://identifiers.org/hco/6/GRCh38#2732255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32946753-C-A

http://identifiers.org/hco/6/GRCh38#2732328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32946811-A-C

2732378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32946860-A-G

2732657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32947126-G-A

2732657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32947126-G-T

2732756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32947218-G-A

2732762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32947225-G-C

2733083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32947527-T-C

2733368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32947891-C-T

2733386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32947907-T-A

2733457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32947974-G-T

2733461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32947978-A-G

2733470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32947989-T-C

2733533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32948048-G-A

2733560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32948079-G-C

2733654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32948130-C-G

2733804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32948253-A-G

http://identifiers.org/hco/6/GRCh38#2734046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32948470-A-C

2734148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32948560-T-C

2734399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32948813-G-A

2734399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32948813-G-C

2734399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32948813-G-T

2734625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32949030-T-C

2734769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32949129-T-C

2734945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32949284-T-A

2734973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32949310-C-G

http://identifiers.org/hco/6/GRCh38#2735243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32949580-A-C

2735434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32949761-G-A

2736139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32950417-G-C

2736644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32950664-C-T

http://identifiers.org/hco/6/GRCh38#2736938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32950964-C-A

2736938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32950964-C-T

2737015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32951037-G-A

http://identifiers.org/hco/6/GRCh38#2737639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32951341-C-A

http://identifiers.org/hco/6/GRCh38#2737649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32951347-A-C

http://identifiers.org/hco/6/GRCh38#2737670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32951368-C-A

2737816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32951513-T-C

2737932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32951653-T-A

http://identifiers.org/hco/6/GRCh38#2737935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32951656-C-A

2737994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32951681-G-A

2737994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32951681-G-T

2738004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32951691-T-A

2738004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32951691-T-G

2738005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32951692-T-A

2738005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32951692-T-G

2738058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32951746-T-C

http://identifiers.org/hco/6/GRCh38#2738245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32951905-C-A

2738316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32951983-G-A

2738598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32952301-C-T

2738938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32952668-G-A

2739449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32954542-G-A

2739449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32954542-G-T

2739846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32955040-C-T

2740409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32956557-G-A

2740661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32956782-G-A

2740661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32956782-G-C

http://identifiers.org/hco/6/GRCh38#2740723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32956855-C-A

2740761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32956891-T-G

2740782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32956912-C-T

2740808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32956932-C-T

2740818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32956974-G-A

2740860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32957021-A-G

2741022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32957192-G-A

2741080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32957230-G-T

http://identifiers.org/hco/6/GRCh38#2741416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32957873-A-C

http://identifiers.org/hco/6/GRCh38#2741816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32958251-C-A

2741816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32958251-C-T

2741853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32958274-G-A

2742075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32958480-G-C

2742077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32958482-T-G

2742491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32958833-G-A

2742737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32959064-A-G

2742748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32959075-T-G

2742902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32959226-G-A

2743424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32959692-A-G

2743602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32959838-T-C

2743881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32960129-A-T

2744049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32960297-G-A

2744049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32960297-G-T

2744080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32960327-T-C

http://identifiers.org/hco/6/GRCh38#2744097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32960344-C-A

2744097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32960344-C-T

2744211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32960461-G-A

2744283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32960536-A-G

2744309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32960562-C-T

2744724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32960968-T-C

2744724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32960968-T-G

2744884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32961396-C-T

2745445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32961802-T-C

2746285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32962473-A-G

2746551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32962737-T-A

2746887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32963051-G-A

2746887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32963051-G-T

2747144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32963292-G-A

2747285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32963402-G-T

2747807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32963752-C-G

2747836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32963788-T-C

2748753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32965085-A-G

2748850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32965164-T-A

http://identifiers.org/hco/6/GRCh38#2748883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32965240-C-A

2748983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32965404-T-C

2748984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32965405-G-A

2748984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32965405-G-T

http://identifiers.org/hco/6/GRCh38#2749065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32965480-C-A

2749065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32965480-C-T

2749114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32965520-G-A

2749114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32965520-G-T

2749183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32965588-G-A

2749241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32965646-C-G

2749241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32965646-C-T

2749414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32965819-G-T

2750073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32967145-T-C

2750078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32967150-A-G

2750466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32967493-A-G

2750585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32967610-A-G

2750618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32967643-G-A

2750618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32967643-G-T

2750623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32967648-G-T

2750627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32967652-T-C

2750841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32967869-C-G

2751485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32968468-G-A

2751586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32968541-A-G

2751606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32968561-G-T

http://identifiers.org/hco/6/GRCh38#2751626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32968580-A-C

2751662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32968616-C-G

2751673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32968625-G-C

2751794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32968757-C-T

2752581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32969291-G-A

2752674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32969331-T-A

2752674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32969331-T-C

2752744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32969402-C-T

2752760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32969418-T-C

http://identifiers.org/hco/6/GRCh38#2752937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32969574-C-A

2753135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32969765-A-T

2753264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32970285-C-G

2753264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32970285-C-T

2753716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32970717-G-C

2754097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32970892-C-G

2754097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32970892-C-T

2754189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32970974-T-C

2754199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32970984-T-C

http://identifiers.org/hco/6/GRCh38#2754271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32971054-A-C

http://identifiers.org/hco/6/GRCh38#2754274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32971057-A-C

2754332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971110-G-A

2754360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971132-T-G

2754498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971257-A-G

2754735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971468-A-G

2754816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32971550-G-A

2755954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32972992-G-A

2755954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32972992-G-T

2755983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973021-G-C

2756217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973241-C-T

http://identifiers.org/hco/6/GRCh38#2756437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32973453-C-A

2756437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973453-C-T

http://identifiers.org/hco/6/GRCh38#2756502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32973521-C-A

2756677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973700-T-C

2756773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973783-C-T

2756786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32973796-T-C

2757134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974149-G-A

2757239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974244-A-G

2757239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974244-A-T

2757362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974384-G-A

2757475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974494-G-C

2757525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974704-A-G

2757566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974862-T-A

2757597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974896-T-A

2757647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32974959-A-G

2757744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975230-T-C

http://identifiers.org/hco/6/GRCh38#2757921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32975434-C-A

2757980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32975490-G-A

2758905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32976220-A-G

2758913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32976228-C-T

2760868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32982600-G-A

2760909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32982627-G-A

2761088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32982781-G-C

2761143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32982826-C-T

2761144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32982827-G-A

2761237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32983010-A-T

2761351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32983116-G-A

2761388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32983153-G-A

2761388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32983153-G-C

2761686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32983465-T-A

2764707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32985456-G-C

2764707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32985456-G-T

http://identifiers.org/hco/6/GRCh38#2764713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#32985460-C-A

2764713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32985460-C-T

2764827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985558-G-C

2764850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985583-A-G

2764955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985674-C-T

2765001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985726-G-A

http://identifiers.org/hco/6/GRCh38#2765016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32985730-C-A

2765016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985730-C-G

2765016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985730-C-T

http://identifiers.org/hco/6/GRCh38#2765167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#32985839-C-A

2765167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32985839-C-G

2765167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32985839-C-T

2765174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32985846-G-C

2765358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32985980-G-T

http://identifiers.org/hco/6/GRCh38#2765406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32986014-C-A

2765406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32986014-C-G

2765406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32986014-C-T

2765452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32986060-G-A

2765452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32986060-G-T

2765550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32986158-A-G

http://identifiers.org/hco/6/GRCh38#2765590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32986189-C-A

2765590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32986189-C-G

2765590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32986189-C-T

http://identifiers.org/hco/6/GRCh38#2765602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32986200-C-A

2765602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32986200-C-T

http://identifiers.org/hco/6/GRCh38#2765665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#32986263-C-A

2765665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 32986263-C-G

2765665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 32986263-C-T

http://identifiers.org/hco/6/GRCh38#2765770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32986368-C-A

2765770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 32986368-C-T

2765862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 32986460-G-A

2765862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 32986460-G-T

http://identifiers.org/hco/6/GRCh38#2765871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32986469-A-C

2765871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 32986469-A-G

http://identifiers.org/hco/6/GRCh38#2766266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32986849-C-A

2766266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 32986849-C-G

2766266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 32986849-C-T

http://identifiers.org/hco/6/GRCh38#2766267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32986850-C-A

2766267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 32986850-C-G

2766267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 32986850-C-T

2766288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 32986871-A-G

2766288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 32986871-A-T

2766321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 32986904-T-C

2766357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 32986940-C-G

2766357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 32986940-C-T

2766475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32987055-T-G

2766510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32987074-A-G

2766540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32987099-C-T

2766676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32987222-A-G

2766686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32987232-T-G

2766693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32987237-A-G

2766837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32987365-T-G

2767378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32987722-A-G

2767576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32987963-A-G

2767815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32988200-A-G

http://identifiers.org/hco/6/GRCh38#2767903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32988282-A-C

2767904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32988283-G-A

2768297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32988954-T-C

2768490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989152-T-C

2768536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989184-C-T

2768555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989185-T-C

http://identifiers.org/hco/6/GRCh38#2768586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32989213-A-C

2768586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989213-A-G

2768586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989213-A-T

2768612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989239-G-T

2768736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, missense_variant
orthologous variants: 32989366-A-G

2768929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989560-A-G

http://identifiers.org/hco/6/GRCh38#2768957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32989596-A-C

2768957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989596-A-G

http://identifiers.org/hco/6/GRCh38#2768960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32989599-C-A

2768960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989599-C-G

2768960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989599-C-T

2768965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989604-G-T

http://identifiers.org/hco/6/GRCh38#2769004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32989649-A-C

2769004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989649-A-G

2769034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989679-A-G

2769034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989679-A-T

2769075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989726-T-C

2769301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32989992-C-T

2769370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32990055-G-A

2769572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32990215-C-G

2769572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32990215-C-T

2769622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32990255-T-C

2769654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32990282-G-A

2769987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32990631-A-G

2770042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32990664-G-A

2770042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron variant
orthologous variants: 32990664-G-T

2770082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, missense_variant
orthologous variants: 32990704-A-G

2770099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32990721-C-T

2770110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: intron_variant, missense_variant
orthologous variants: 32990732-C-T

http://identifiers.org/hco/6/GRCh38#2770170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#32990792-A-C

2770170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 32990792-A-T

2770201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 32990823-G-A

2770221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 32990843-T-C

2770359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27972
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 32990981-A-G