http://identifiers.org/hco/17/GRCh38#64147478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#106393006-C-A

64147550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106393060-A-G

64147601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106393102-G-T

http://identifiers.org/hco/17/GRCh38#64147634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106393136-C-A

64147634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106393136-C-T

64147900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106393385-G-A

64147900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106393385-G-T

http://identifiers.org/hco/17/GRCh38#64148278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106393739-C-A

64148729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106394184-G-T

64148731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106394186-T-A

64148731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106394186-T-C

64148773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106394225-G-A

64148773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106394225-G-T

64148855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106394303-C-T

64148871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106394319-G-T

64148894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106394346-A-G

64148936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106394388-T-G

http://identifiers.org/hco/17/GRCh38#64149145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106394584-C-A

http://identifiers.org/hco/17/GRCh38#64149147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106394586-C-A

64149147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106394586-C-T

64149948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106395761-G-A

64150226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397186-G-A

64150226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397186-G-T

64150303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397273-G-T

64150366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397305-G-T

64150376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397315-T-C

64150414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397345-G-C

64150431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397362-T-A

64150431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397362-T-G

64150461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397379-G-A

64150461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397379-G-C

64150461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397379-G-T

http://identifiers.org/hco/17/GRCh38#64150538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106397452-A-C

64150538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397452-A-G

64150538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397452-A-T

64150552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397467-G-T

64150662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397568-G-A

64150662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397568-G-T

http://identifiers.org/hco/17/GRCh38#64150774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106397636-C-A

64150774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106397636-C-T

64150984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106397835-C-T

http://identifiers.org/hco/17/GRCh38#64151132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106397972-C-A

64151281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106398119-T-C

64152498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106402179-G-A

64152501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106402182-G-A

64152612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106402264-C-T

64152629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106402281-A-G

64152899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106402694-T-C

64152942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106402725-C-T

64153139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106402922-A-G

64153174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106402957-A-G

64153395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106403231-T-C

64153428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106403271-C-T

64153445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106403285-C-G

64154190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106403853-C-T

64154229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106403891-T-C

64154394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106404055-G-A

64154483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106404132-C-T

64154484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106404133-A-G

http://identifiers.org/hco/17/GRCh38#64154515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106404157-A-C

64154722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106404309-A-G

64154722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106404309-A-T

64154809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106404388-G-C

64154809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106404388-G-T

64154994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404565-T-A

64154994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404565-T-G

64155024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404569-A-G

http://identifiers.org/hco/17/GRCh38#64155039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106404584-C-A

http://identifiers.org/hco/17/GRCh38#64155041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106404586-A-C

64155041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404586-A-G

64155042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404587-T-A

64155042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404587-T-C

64155099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404634-T-C

64155100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404635-T-C

64155261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404772-G-A

64155261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404772-G-T

64155304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404810-T-A

64155353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404855-G-A

64155353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404855-G-C

64155353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404855-G-T

64155354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404856-A-G

http://identifiers.org/hco/17/GRCh38#64155469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106404942-A-C

64155525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106404989-T-C

64155608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106405066-C-G

http://identifiers.org/hco/17/GRCh38#64155652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106405096-A-C

64155652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106405096-A-T

64155675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106405121-T-A

64155778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106405226-A-G

64155813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106405243-T-C

64155813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106405243-T-G

64155882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106405283-G-T

64156107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106405497-G-T

64156127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106405517-G-A

64156127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106405517-G-T

64156270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106405611-C-T

http://identifiers.org/hco/17/GRCh38#64156323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#106405664-C-A

http://identifiers.org/hco/17/GRCh38#64156331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#106405672-C-A

64156331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106405672-C-G

http://identifiers.org/hco/17/GRCh38#64156365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#106405702-C-A

64156365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106405702-C-G

64156530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106405846-G-A

64156664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106405981-C-G

64156751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106406051-C-T

64158203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106408342-A-T

64158328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106408427-G-A

64158483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106408576-C-T

64158601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106408676-G-A

64158699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106408775-A-G

64158784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106408801-G-A

64158937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106408929-T-A

64158943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106408935-A-G

64159158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409124-C-G

64159165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409135-C-T

64159167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409137-G-A

64159302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409267-T-C

64159539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409589-C-T

http://identifiers.org/hco/17/GRCh38#64159575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106409615-C-A

64159575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409615-C-G

64159575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409615-C-T

64159631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409669-C-T

64159677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409714-G-A

64159707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409742-T-C

64159749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409787-G-C

64159755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409793-T-C

64159778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409814-C-T

64159844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409874-T-C

64159914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409944-C-G

64159914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106409944-C-T

http://identifiers.org/hco/17/GRCh38#64160383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106410331-C-A

64160652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106410569-A-T

http://identifiers.org/hco/17/GRCh38#64160656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106410573-C-A

64160656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106410573-C-T

64160674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106410584-A-G

http://identifiers.org/hco/17/GRCh38#64160718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106410627-C-A

64160718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106410627-C-T

http://identifiers.org/hco/17/GRCh38#64160723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106410632-C-A

64160723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106410632-C-T

64160878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106410785-C-T

64161014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106410938-C-G

64161014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106410938-C-T

http://identifiers.org/hco/17/GRCh38#64161039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106410953-C-A

64161039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106410953-C-G

64161039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106410953-C-T

http://identifiers.org/hco/17/GRCh38#64161055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106410969-C-A

64161061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106410975-T-A

64161883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106412838-A-G

64161981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106412935-C-T

http://identifiers.org/hco/17/GRCh38#64162160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106413109-A-C

64162206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106413147-T-C

64163691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106414604-T-C

64165103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106416502-T-C

64168563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106417914-A-G

64168670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106418033-A-G

64168854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106418226-G-A

64168856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106418228-T-C

64169512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106418465-G-A

64169631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106418545-T-A

64170149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106419092-C-T

64170164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106419107-T-C

64170185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106419126-G-A

64170302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106419237-G-A

64170386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106419320-G-A

64170459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106419375-G-A

64170459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106419375-G-T

64170473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106419390-G-T

64171001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106419986-A-T

64171003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106419991-A-G

64171038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106420015-G-A

64171038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106420015-G-T

64172452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106420629-C-T

64172513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106420697-T-C

64172903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421021-T-A

64172930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421053-T-C

64173153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421572-T-C

64173260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106421816-G-T

64174682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106422731-G-A

64174682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106422731-G-C

64175261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106422954-T-C

64175419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106423099-G-A

64175471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106423140-T-C

64175490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106423156-G-A

64175749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106423242-G-C

64176147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106423525-C-G

64176386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106423740-G-A

64176459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106423814-A-G

64176493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106423841-C-T

64176680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106424021-A-T

64176713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106424063-C-T

64176741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106424090-T-C

64177071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106424477-G-C

64177071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106424477-G-T

http://identifiers.org/hco/17/GRCh38#64177213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106424591-C-A

64177361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106424733-C-G

64177361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106424733-C-T

64177488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106424860-G-A

64177488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106424860-G-T

64177572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106424943-A-G

64177589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106424957-A-G

http://identifiers.org/hco/17/GRCh38#64177888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106425247-A-C

64177978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106425313-T-C

64178334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106425626-T-C

64178530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106425834-T-A

64178662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106425949-A-G

64178848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106426120-G-T

64178870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106426139-A-G

64179907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106426790-C-G

64179985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106426869-G-C

http://identifiers.org/hco/17/GRCh38#64180011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106426904-C-A

64180011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106426904-C-T

64180253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106427135-C-T

64180288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106427169-G-A

64180645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106427483-G-A

64180664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106427502-G-A

http://identifiers.org/hco/17/GRCh38#64180981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106427798-C-A

64181015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106427836-G-A

64181046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106427866-C-T

64185053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106431283-T-G

64185060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106431290-T-C

64185070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106431295-G-A

64185074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106431299-C-G

64185108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106431327-A-G

http://identifiers.org/hco/17/GRCh38#64185364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106431590-C-A

64185435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106431663-T-G

64185499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106431720-C-T

http://identifiers.org/hco/17/GRCh38#64186197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106433810-A-C

64186369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106433971-T-C

64186395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106433989-G-A

64186571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434169-C-G

64186571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434169-C-T

http://identifiers.org/hco/17/GRCh38#64188031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106434865-C-A

http://identifiers.org/hco/17/GRCh38#64188032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106434866-C-A

64188032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434866-C-T

http://identifiers.org/hco/17/GRCh38#64188064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106434899-C-A

64188064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434899-C-T

64188065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434900-A-T

http://identifiers.org/hco/17/GRCh38#64188075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106434910-C-A

64188075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434910-C-T

http://identifiers.org/hco/17/GRCh38#64188106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106434948-C-A

64188106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434948-C-G

64188106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434948-C-T

64188110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434952-T-A

64188110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434952-T-G

64188136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434970-T-C

64188136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434970-T-G

http://identifiers.org/hco/17/GRCh38#64188142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106434976-A-C

64188142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434976-A-G

64188144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434978-G-A

64188144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434978-G-T

64188151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106434985-C-T

64188207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106435037-G-A

64188215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106435045-T-A

64188215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106435045-T-C

64188231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106435061-T-C

64188261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106435091-G-A

64188291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106435121-G-A

64188436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 106435263-G-A

64188436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 106435263-G-C

64188436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 106435263-G-T

http://identifiers.org/hco/17/GRCh38#64189098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106435592-A-C

64189148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106435639-T-C

64189221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106435722-A-G

64189505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106435888-G-C

64190692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106436542-T-C

64190858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106436679-A-G

64190859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106436680-G-A

64190859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106436680-G-C

64191045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106436853-G-A

64191259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106437036-G-A

64193425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106437361-T-A

64193425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106437361-T-C

64193502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106437436-C-T

http://identifiers.org/hco/17/GRCh38#64193532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106437465-A-C

64193532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106437465-A-T

http://identifiers.org/hco/17/GRCh38#64193581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106437512-C-A

64193581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106437512-C-G

64193581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106437512-C-T

http://identifiers.org/hco/17/GRCh38#64193893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106437833-C-A

64193893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 106437833-C-T

http://identifiers.org/hco/17/GRCh38#64193973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106437913-C-A

64193973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106437913-C-T

64193977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106437917-A-G

64194006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106437942-G-T

http://identifiers.org/hco/17/GRCh38#64194022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106437957-C-A

64194022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106437957-C-T

http://identifiers.org/hco/17/GRCh38#64194038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106437972-C-A

64194762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106439405-G-C

64194762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106439405-G-T

64194931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106439576-G-A

http://identifiers.org/hco/17/GRCh38#64195854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106441827-A-C

64196360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106442547-G-A

64196506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106442645-G-T

64196616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106442780-T-C

64200447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106446795-C-G

64200472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106446803-C-T

64200821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106447045-G-A

64200836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106447059-G-A

64201277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106447420-C-T

64201512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106447643-G-A

64201830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106447893-T-C

64202380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106448254-C-G

64202638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106448495-G-A

64202714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106448572-G-T

64202740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106448597-T-C

64203066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106448907-G-A

64203707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106449479-T-G

64206130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106450992-G-A

64206293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106451126-G-A

64206391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106451197-A-G

64206533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106451325-G-A

64207023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106451486-G-A

64207629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106453598-G-A

64207655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106453624-C-G

64209785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106454893-G-A

64209785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106454893-G-T

64210175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106455192-C-T

64210304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106455318-T-C

64210637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106455587-T-A

64210637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106455587-T-C

64210876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106455829-T-C

64210917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106455872-G-A

64212611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: missense variant
orthologous variants: 106457828-G-T

64212714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: missense variant
orthologous variants: 106457931-T-C

http://identifiers.org/hco/17/GRCh38#64212730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106457947-A-C

64212730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106457947-A-G

http://identifiers.org/hco/17/GRCh38#64212799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106458016-C-A

64213093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106458310-C-T

64213109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: missense variant
orthologous variants: 106458326-G-A

64213270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106458484-A-G

64213306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106458520-G-A

64213306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106458520-G-T

64213429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106458643-T-A

64213429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106458643-T-C

64213450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106458664-T-A

64213450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106458664-T-C

64213627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106458841-G-A

64213627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106458841-G-T

64213684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106458898-T-G

64213735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: synonymous variant
orthologous variants: 106458949-G-A

64213920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: missense variant
orthologous variants: 106459134-C-T

64213955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: missense variant
orthologous variants: 106459166-G-A

64214133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: missense variant
orthologous variants: 106459344-C-T

64214354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106459558-A-G

64214389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106459593-G-T

64214458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106459665-G-A

http://identifiers.org/hco/17/GRCh38#64214520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106459724-A-C

64215163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106460234-C-T

64215278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106460488-G-A

64215440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106460648-G-A

64215545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106460748-C-T

64215578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106460780-G-C

64215601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106460804-T-G

64215645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106460867-T-G

64215709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106460922-G-A

http://identifiers.org/hco/17/GRCh38#64215740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106460953-A-C

64215744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106460957-G-A

http://identifiers.org/hco/17/GRCh38#64215791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106461008-C-A

64215903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106461074-G-A

64216170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106461296-G-A

64216272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106461551-T-C

64216540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106462000-G-A

64216540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106462000-G-T

64216962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, undefined
orthologous variants: 106462393-T-C

64216972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, undefined
orthologous variants: 106462405-C-T

http://identifiers.org/hco/17/GRCh38#64217018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106462454-C-A

64217177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106462708-C-T

64217194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106462723-G-A

64217330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106462840-C-T

64217444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106462929-G-A

http://identifiers.org/hco/17/GRCh38#64217564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106463022-C-A

64217649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106463111-C-G

64218054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106463486-C-T

64223091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106464859-G-A

64223095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106464863-C-T

http://identifiers.org/hco/17/GRCh38#64223251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106465037-C-A

64223251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106465037-C-T

64223568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106465315-T-G

http://identifiers.org/hco/17/GRCh38#64223759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106465360-A-C

http://identifiers.org/hco/17/GRCh38#64223808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106465393-C-A

64224145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106465541-T-G

64224374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106465841-G-A

64224671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106466160-G-A

64229740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106468381-G-C

64229815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106468462-T-C

64230041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106468640-G-C

64230399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106469647-C-T

64230466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106469705-C-T

http://identifiers.org/hco/17/GRCh38#64230475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106469714-C-A

64230523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106469746-G-A

64230523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106469746-G-T

http://identifiers.org/hco/17/GRCh38#64230524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106469747-C-A

64230524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106469747-C-T

64230605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, undefined
orthologous variants: 106469857-A-G

64230735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106469952-G-T

64231132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron_variant, undefined
orthologous variants: 106470332-A-G

64231964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106472891-T-C

64231973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106472900-G-C

64232351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106474078-T-A

64233152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106474986-G-A

64233257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: -A-G

64233791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106475754-T-C

64233794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106475761-A-G

64234258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106476370-T-C

64234391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106476497-T-C

64234391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106476497-T-G

64234510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106476601-T-C

64234512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106476603-C-T

64234520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106476611-A-G

64235228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106478241-G-C

http://identifiers.org/hco/17/GRCh38#64235349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106478346-A-C

64235387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106478380-G-T

64235719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106478873-C-T

64235764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106478923-C-T

64235765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106478924-A-G

64236050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106479217-T-C

64236815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106479375-T-C

64237008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106479534-G-A

64237008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106479534-G-C

64237072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106479562-A-G

64237102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106479590-C-T

64237140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106479628-G-C

64237141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106479629-T-C

64237359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106479778-G-T

64237566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106479905-G-A

64237566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106479905-G-C

64237660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106479983-G-T

64237788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106480108-T-C

http://identifiers.org/hco/17/GRCh38#64237827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106480146-A-C

64237854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106480173-T-G

64239124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106480711-A-G

64239144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106480731-C-T

64239345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106481059-G-T

64239351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106481065-T-A

64239493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106481397-C-T

64239988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106481575-A-G

64244340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106483787-C-T

64244573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106484022-C-G

64244573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106484022-C-T

64244757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106484407-A-T

64244769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106484419-T-C

64244796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106484442-T-C

64245527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106485232-T-C

64245610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106485347-A-G

64246041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106486183-C-T

64246102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106486234-A-G

64246625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106486462-G-A

64246855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106486692-G-A

64248359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106488508-T-G

64248448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106488680-G-C

64248967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106489051-G-A

64248981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106489065-G-A

64249053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106489112-G-A

http://identifiers.org/hco/17/GRCh38#64249326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106489359-A-C

64249591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106489935-G-A

64249932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106490302-C-T

64250110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106490481-G-A

http://identifiers.org/hco/17/GRCh38#64250274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106490800-A-C

64250826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106491119-T-C

64250994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106491223-C-T

64251106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106491341-G-A

64251161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106491387-A-G

64252723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106493164-T-C

64252803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106493241-A-G

64252845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106493283-G-A

64252887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106493329-T-G

64253252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106493645-C-T

64253327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106493712-T-G

http://identifiers.org/hco/17/GRCh38#64253362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106493757-A-C

64253362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106493757-A-T

64253370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106493765-G-T

http://identifiers.org/hco/17/GRCh38#64253387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106493782-A-C

64253442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106493843-G-A

64253646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106493975-C-T

64253647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106493976-G-A

64253704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106494023-G-A

http://identifiers.org/hco/17/GRCh38#64253777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106494104-C-A

64253966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106494273-T-C

64254328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106494562-T-C

64254503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106494856-C-T

64254526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106494878-C-T

64255784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106496532-T-A

64255791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106496539-G-A

64255808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106496556-A-G

64255883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106496618-T-C

64255960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 106496711-C-T

64256037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106496808-A-G

64256499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106497285-C-T

64256519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106497307-T-C

64256643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106497390-A-G

64256789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106497534-T-C

64257106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106497852-G-A

64257106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106497852-G-C

64257182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106497924-G-A

64258641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106499588-A-T

64259258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106499958-G-C

64259525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500222-A-G

64259583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500280-T-C

64259585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500282-G-C

64259628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500339-T-C

64259629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500340-G-C

64259643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500354-G-A

64259707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500416-G-A

64259727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500435-T-C

64259748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500457-G-C

64259795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500507-T-C

64260038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500737-G-T

64260073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500774-T-C

64260114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500807-T-C

64260127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500820-T-G

http://identifiers.org/hco/17/GRCh38#64260232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106500909-C-A

64260270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106500932-C-G

64260637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106501203-G-T

64261873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106502547-T-C

64262227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106502794-G-A

64262268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106502828-G-A

64262490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106503068-G-T

64262496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106503074-T-C

http://identifiers.org/hco/17/GRCh38#64262631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106503181-C-A

64262631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: intron variant
orthologous variants: 106503181-C-T

64262976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106503529-G-T

64262995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106503548-T-A

64263043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106503584-G-A

64263043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106503584-G-C

64263043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106503584-G-T

64263089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106503625-G-A

64263099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106503628-G-A

64263138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106503655-C-T

64263155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106503671-T-A

64263155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106503671-T-C

64263199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5 prime UTR variant
orthologous variants: 106503715-G-A

64263199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5 prime UTR variant
orthologous variants: 106503715-G-T

64263201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5 prime UTR variant
orthologous variants: 106503717-C-G

64263201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30884
most severe consequence: 5 prime UTR variant
orthologous variants: 106503717-C-T