64095032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100229071-T-C

64095052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100229091-A-G

64095238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100229253-A-G

64095594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100229601-T-A

64095748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100229765-A-G

64095804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100229818-T-A

64095973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100229978-C-G

64096137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100230139-T-C

http://identifiers.org/hco/1/GRCh38#64097034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100230298-C-A

64097113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100230375-G-T

64097287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100230510-C-T

64097643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100230827-A-G

http://identifiers.org/hco/1/GRCh38#64097661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100230845-C-A

64097848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100231014-A-G

64098112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100231240-C-T

64098118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100231247-A-G

64098141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100231284-G-A

64098249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100231374-A-T

64098291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100231409-A-G

64098465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100231608-C-G

64098568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100231740-G-T

64098668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100231891-A-G

http://identifiers.org/hco/1/GRCh38#64098709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100232048-C-A

64099042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100232367-A-G

64099072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100232399-G-A

64099133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100232465-A-G

64099135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100232467-C-T

64099173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100232513-G-A

64099196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100232536-C-T

http://identifiers.org/hco/1/GRCh38#64099285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100232602-A-C

64099285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100232602-A-G

64099319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100232626-G-A

64099662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100232924-C-T

64100545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100233289-T-C

64100673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100233416-C-T

64101007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100233717-A-G

64101086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100233801-T-C

64101182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100233893-G-A

64101362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100234047-A-G

64101626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100234256-C-T

64102151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100234721-C-T

64102265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100234818-C-T

64102392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100234929-A-G

64102499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100235034-G-A

64102548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100235082-C-T

64102639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100235156-T-G

64102801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100235276-A-G

64102836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100235312-A-G

64102938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100235400-T-A

64103023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100235484-C-T

64103117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100235576-G-A

64109907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100235967-T-A

64110045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100236095-C-T

64110132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100236178-A-T

64110198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100236242-G-A

64110434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100236476-T-C

64110754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100236731-A-G

64110763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100236740-G-T

64110791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100236762-G-A

64110791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100236762-G-T

64110813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100236783-T-G

http://identifiers.org/hco/1/GRCh38#64110846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100236811-C-A

64111023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100236950-A-G

64111023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100236950-A-T

64111116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100237044-A-G

64111298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100237209-G-T

64111533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100237421-C-T

64111662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100237557-G-A

64111698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100237593-A-G

http://identifiers.org/hco/1/GRCh38#64111860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100237755-C-A

http://identifiers.org/hco/1/GRCh38#64111862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100237757-C-A

64112106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100238009-G-T

64112298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100238198-G-T

64112304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100238206-T-C

64112459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100238339-C-T

64112850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100238604-C-T

64113148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100238893-T-C

64113430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100239183-A-G

http://identifiers.org/hco/1/GRCh38#64113569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100239292-C-A

64113588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100239312-A-G

64113597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100239321-A-G

64113633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100239348-G-T

64113696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100239412-G-T

64113707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100239423-G-C

64113707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100239423-G-T

http://identifiers.org/hco/1/GRCh38#64113759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100239476-C-A

64113759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100239476-C-T

http://identifiers.org/hco/1/GRCh38#64113841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100239550-C-A

64113841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100239550-C-T

64114017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100239721-A-G

64114150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100239850-G-A

http://identifiers.org/hco/1/GRCh38#64114181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100239884-A-C

64114230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100239928-A-G

64114527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100240186-G-A

64114677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100240315-A-G

http://identifiers.org/hco/1/GRCh38#64114901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100240575-C-A

64114901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100240575-C-T

64115123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100240620-G-C

64115166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100240659-G-C

64115820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100241253-C-T

64116057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100241513-G-A

64116074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100241530-C-G

64116199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100241653-T-C

64116279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100241731-T-C

64116453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100241909-A-G

64116502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100241949-A-G

64116731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100242210-A-T

64116837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100242282-T-A

64116892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100242337-T-C

64116948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100242374-A-G

64116948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100242374-A-T

64117136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100242583-G-C

64117136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100242583-G-T

64117178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100242617-G-A

64117502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100242948-G-A

64117886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100243297-G-A

64118820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100243540-T-A

64118937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100243629-A-T

64119027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100243697-A-G

64119132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100243795-T-C

64119192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100243857-G-A

64119302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100243965-T-A

64121734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100247549-C-T

http://identifiers.org/hco/1/GRCh38#64121787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100247602-C-A

64122180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100247961-T-C

64122180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100247961-T-G

64122189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100247970-A-G

64122202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100247988-T-C

64122296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100248066-G-T

64122466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100248181-A-G

http://identifiers.org/hco/1/GRCh38#64122675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100248329-A-C

64122722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100248372-G-A

64122863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100248510-C-T

64122919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100248567-G-C

64123063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100248889-C-T

64123161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100249047-C-G

64123264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100249146-C-G

64123264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100249146-C-T

64123284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100249169-C-T

64123374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100249254-G-A

http://identifiers.org/hco/1/GRCh38#64123539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100249409-A-C

http://identifiers.org/hco/1/GRCh38#64123617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100249483-A-C

64123626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100249492-T-C

64123626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100249492-T-G

http://identifiers.org/hco/1/GRCh38#64123676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100249537-A-C

64123679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100249540-G-A

64123757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100249608-A-G

64123856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100250112-C-T

64123925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100250178-C-T

64124522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100250665-G-T

64124796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100250920-A-G

64124993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100251117-C-T

64125502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100251626-A-G

http://identifiers.org/hco/1/GRCh38#64125551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100251678-C-A

64125554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100251681-A-G

64125679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100251802-A-G

64125805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100251929-C-G

64125893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100252017-C-T

64126018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100252156-G-A

http://identifiers.org/hco/1/GRCh38#64126097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100252233-C-A

64126097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100252233-C-T

64126278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100252379-T-A

64126715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100252799-C-T

64126811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100252894-G-A

64126825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100252908-T-C

64126950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100253053-C-T

64126980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100253083-C-G

64127251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100253784-T-C

64127283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100253816-A-G

64127333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100253850-A-G

64127892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100254152-G-A

64127914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100254173-C-T

http://identifiers.org/hco/1/GRCh38#64127955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100254215-C-A

64128034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100254288-G-T

64129013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100258071-T-C

64129082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100258130-G-A

64129428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100258506-A-T

64129457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100258535-G-A

64129703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100258776-G-A

64130002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100259074-A-G

64130076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100259151-G-A

64130081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100259156-G-A

64130422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100259468-A-G

64130562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100259576-A-G

64130705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100259709-C-T

64134517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100261831-G-T

64135064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100262332-G-T

64135077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100262344-A-G

64135089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100262370-G-T

64135206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100262514-T-C

64135484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100262790-G-T

64137238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100264862-T-C

64137239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100264863-A-T

http://identifiers.org/hco/1/GRCh38#64137298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#100264945-C-A

64137298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100264945-C-G

64137298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100264945-C-T

64137299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100264946-G-A

64137299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100264946-G-T

64137322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100264964-G-A

64137322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100264964-G-C

64137322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100264964-G-T

64137323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100264965-T-C

64137327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100264969-T-A

64137327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100264969-T-C

64137417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100265058-A-G

64137489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100265130-G-T

64137762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100265405-A-G

64137785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100265426-A-G

64137824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100265466-C-T

64139198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100265962-G-T

64139205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100265969-T-C

64139373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100266163-T-G

64139400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100266190-G-C

http://identifiers.org/hco/1/GRCh38#64139590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100266390-C-A

64139648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100266448-A-G

64139678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100266478-C-T

http://identifiers.org/hco/1/GRCh38#64139711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100266501-C-A

64139877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100266683-G-T

http://identifiers.org/hco/1/GRCh38#64140055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100266858-C-A

http://identifiers.org/hco/1/GRCh38#64140459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100267249-C-A

64140460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100267250-T-A

64140465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100267255-G-T

64140487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100267276-G-A

64140487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100267276-G-C

http://identifiers.org/hco/1/GRCh38#64140505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100267291-C-A

64140505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100267291-C-T

64140506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100267292-A-G

64140551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100267319-A-G

64140557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100267325-G-A

64140557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100267325-G-T

64140603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100267371-G-A

64141657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100268474-T-C

64141865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100268556-C-T

64142080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100268729-C-G

64142188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100268845-A-G

64142251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100268907-C-G

64142265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100268916-T-C

64142271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100268922-G-A

64142271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100268922-G-T

64142356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100269042-C-G

64142356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100269042-C-T

64142792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100269451-C-T

http://identifiers.org/hco/1/GRCh38#64142901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#100269565-C-A

64142901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100269565-C-G

64142901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100269565-C-T

64142911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100269575-G-A

64142911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100269575-G-T

64142957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100269624-T-C

64143006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100269670-A-T

64143127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100269787-G-T

64143381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100269888-G-A

64143381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100269888-G-C

64143381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100269888-G-T

64143388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100269895-T-A

64143388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100269895-T-C

64143388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100269895-T-G

64143514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100270011-A-G

64143526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100270023-T-C

64143719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100270197-C-T

64143724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100270202-A-G

64143871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100270328-T-C

64143892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100270349-G-C

64144157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100270498-A-G

64144210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100270544-A-G

64144231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100270564-G-A

64146554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100270783-T-C

64146627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100270849-G-A

64146925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100271012-G-A

64147470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100271540-A-G

http://identifiers.org/hco/1/GRCh38#64147505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100271574-A-C

64147511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100271582-G-A

64147576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100271623-G-A

64147874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100272035-T-C

64148053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100272210-A-T

64148088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100272245-G-A

64148088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100272245-G-C

64148101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100272260-A-G

64148157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100272315-G-T

64148201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100272352-A-G

64148267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100272464-G-A

64148642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100273116-G-A

64148720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100273190-T-C

64148981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100273450-G-A

64149045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100273521-T-A

64149073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100273558-C-G

64149137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100273624-C-T

64149139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100273626-G-A

64149337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100273813-G-A

64149473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100273946-A-T

64149815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100274195-C-T

http://identifiers.org/hco/1/GRCh38#64149826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100274206-C-A

64149862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100274249-C-G

64149862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100274249-C-T

64149978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100274357-T-C

64150150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100274519-C-T

64150553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100274904-T-C

64150725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100275060-G-A

64151962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100276314-C-G

64152277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100276537-T-G

64152510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100276745-G-A

64153113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100277255-G-A

64153178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100277362-A-G

64153195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100277379-A-T

64153202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100277386-C-G

64153536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100277986-A-G

64153540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100277990-G-A

64153961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100278389-G-A

64153965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100278393-A-G

64153980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100278406-G-A

64154031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100278451-T-C

64154084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100278500-T-G

64154196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100278601-C-T

64154708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100279142-A-T

64154778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100279212-T-G

64154783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100279217-G-T

64154906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100279333-T-C

64154968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100279399-T-C

64155527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100280182-C-T

64155580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100280237-A-G

64156232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100280917-G-C

64156248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100280933-G-A

64156365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100281114-G-A

64157725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100281839-G-A

64157924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100282031-A-G

64157924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100282031-A-T

64158078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100282191-A-G

64158432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100282563-C-T

64158689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100282841-G-C

64158971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100283101-C-T

64159087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100283217-C-G

64159180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100283310-A-G

64159180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100283310-A-T

http://identifiers.org/hco/1/GRCh38#64159231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100283340-C-A

64159843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100283902-T-A

64160020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100284073-T-A

64160229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100284254-C-G

64160229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100284254-C-T

64160393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100284424-A-G

64160412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100284444-G-A

64160549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100285652-A-G

64160865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100285879-C-T

64161053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100286098-T-G

64161079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100286121-A-G

64161238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100286437-T-C

64161300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100286513-C-T

64161374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100286578-G-A

64161410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100286593-T-C

http://identifiers.org/hco/1/GRCh38#64161519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100286689-C-A

64161519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100286689-C-T

64161559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100286725-T-C

http://identifiers.org/hco/1/GRCh38#64161794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100286967-A-C

64161794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100286967-A-G

64161834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100287005-T-G

64162086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100287224-C-T

64162088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100287226-G-C

64162198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100287339-G-A

64162390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100287542-C-G

64162390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100287542-C-T

64162391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100287543-G-A

64162769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100287872-C-T

64162987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100288050-G-A

64162991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100288054-G-A

64162991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100288054-G-C

64162991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100288054-G-T

64162993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100288056-G-A

64163068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100288062-T-G

64163080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100288074-G-A

64163088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100288082-A-G

64163091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100288085-A-T

64163092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100288086-T-C

64163096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100288090-G-A

64163236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100288120-C-G

http://identifiers.org/hco/1/GRCh38#64163242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100288126-C-A

64163516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100288296-T-G

64163629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100288405-T-G

64164172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100289015-G-T

64164208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100289050-C-G

64164275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100289105-A-G

64164544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100289410-G-T

64166671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100289544-G-A

64166915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100289708-A-G

64167029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100289831-G-C

http://identifiers.org/hco/1/GRCh38#64167506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100290542-A-C

64167637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100290665-A-G

64167777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100290786-T-C

64167807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100290801-A-G

64168085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100291059-G-A

64169138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100291761-A-G

64169157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100291769-G-T

64169192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100291814-G-A

64169192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100291814-G-T