52931411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112774-T-C

52931482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112708-A-G

http://identifiers.org/hco/5/GRCh38#52931513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115112684-A-C

52931513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112684-A-G

52931513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112684-A-T

http://identifiers.org/hco/5/GRCh38#52931538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115112662-C-A

52931538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112662-C-G

52931538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112662-C-T

52931570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112630-G-T

52931605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112595-G-C

52931605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112595-G-T

52931614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112586-T-C

52931648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112552-T-A

52931648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112552-T-C

52931686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112540-A-G

52931776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112469-G-A

52931776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112469-G-T

52931777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112468-G-A

52931777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112468-G-T

52931839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112405-G-A

http://identifiers.org/hco/5/GRCh38#52931885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115112372-C-A

52931885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112372-C-G

52931885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112372-C-T

http://identifiers.org/hco/5/GRCh38#52931905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115112352-C-A

52931932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112327-A-T

52931951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112309-T-C

52931951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112309-T-G

52931959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112301-A-G

52932006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112256-A-G

52932015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112249-T-C

52932018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112246-T-A

52932030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112234-T-C

52932045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112223-A-G

http://identifiers.org/hco/5/GRCh38#52932072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115112196-C-A

52932072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 115112196-C-T

52932102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 115112166-C-T

52932140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112128-G-A

52932162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112106-G-A

52932162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112106-G-T

52932163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112105-G-T

52932174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112094-A-G

52932178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112090-A-T

http://identifiers.org/hco/5/GRCh38#52932222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115112056-C-A

52932222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115112056-C-T

52932281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111970-C-G

52932288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111963-T-A

52932288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111963-T-C

http://identifiers.org/hco/5/GRCh38#52932478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115111780-C-A

52932478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111780-C-G

52932478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111780-C-T

52932538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111717-T-C

52932563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111693-T-C

52932612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111649-C-T

52933302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111338-T-A

52933302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111338-T-C

52933421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111217-A-G

http://identifiers.org/hco/5/GRCh38#52933437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115111202-C-A

http://identifiers.org/hco/5/GRCh38#52933438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115111201-C-A

52933438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111201-C-T

52933532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111115-A-G

http://identifiers.org/hco/5/GRCh38#52933543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115111095-C-A

52933543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111095-C-T

52933576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115111050-T-G

52933805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110819-A-G

52933817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110807-T-C

52933817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110807-T-G

52933820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110804-A-G

52933820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110804-A-T

52933842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110782-A-G

52933842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110782-A-T

52933866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110761-T-C

52933882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110742-T-A

52933882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110742-T-C

52933931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110692-G-A

52933931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110692-G-T

http://identifiers.org/hco/5/GRCh38#52933940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115110683-C-A

52933940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110683-C-T

52933958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110665-A-G

52934005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110618-T-C

52934020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110603-T-A

52934020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110603-T-C

http://identifiers.org/hco/5/GRCh38#52934097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115110550-A-C

52934097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110550-A-G

52934114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110533-T-G

52934297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110365-A-G

52934337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110333-G-A

52934613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115110048-A-G

52934691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115109985-A-G

52934713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115109963-G-A

http://identifiers.org/hco/5/GRCh38#52934798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115109883-C-A

http://identifiers.org/hco/5/GRCh38#52934827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115109852-A-C

52935069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115109658-T-C

52935079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115109648-C-G

52935079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115109648-C-T

52935295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115109404-T-A

52935589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115109169-A-G

52935661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115109106-C-T

52935700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115109059-T-C

52935742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115109023-A-G

52935775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115108993-T-A

52935892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115108858-T-C

http://identifiers.org/hco/5/GRCh38#52935947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115108804-C-A

52935951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115108800-G-T

52935955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115108796-T-G

52936378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115108676-A-T

52936513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115108549-T-A

52936513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115108549-T-C

52936591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115108467-G-C

52936612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115108445-C-T

52936801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115108365-G-A

52936846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115108324-C-T

52936897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115108274-G-T

52937351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115107178-A-G

52937376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115107152-T-C

52937494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115107033-A-G

52937523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115107004-T-C

52937566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115106669-T-C

52937598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115106637-G-A

52937598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115106637-G-T

52937777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115106447-G-T

http://identifiers.org/hco/5/GRCh38#52937780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115106444-A-C

52937934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115106349-A-G

52937953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115106333-T-C

52938093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115106196-A-T

52938116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115106171-T-C

52938516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115105715-G-A

52939485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115105198-T-C

52939487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115105196-T-A

52939495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115105188-G-A

52939495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115105188-G-T

52939497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115105186-T-C

52939502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115105181-T-C

52939502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115105181-T-G

52939503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115105180-T-C

http://identifiers.org/hco/5/GRCh38#52939519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115105164-C-A

52939611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115105074-A-G

52939722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104961-T-C

http://identifiers.org/hco/5/GRCh38#52939781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115104901-A-C

52939781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104901-A-T

52939809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104872-T-A

http://identifiers.org/hco/5/GRCh38#52939845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115104837-C-A

52939845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104837-C-G

52939845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104837-C-T

52939950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104732-T-A

52939950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104732-T-C

52939959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104728-A-G

52939962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104723-T-C

http://identifiers.org/hco/5/GRCh38#52939969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115104716-A-C

52939973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104712-A-G

52940024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104698-T-A

52940024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104698-T-G

52940032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104691-T-C

52940036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104687-G-A

52940036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104687-G-T

52940053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104670-G-A

52940053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104670-G-T

52940152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104594-C-T

52940153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104593-C-T

52940223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104540-C-T

52940234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104529-G-A

52940427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104269-G-T

52940493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104215-C-G

52940534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104173-G-A

52940551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115104158-G-A

http://identifiers.org/hco/5/GRCh38#52944614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115103990-C-A

52944614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115103990-C-T

52944658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115103951-C-T

52944715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115103894-T-A

52944716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115103893-T-C

52944839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115103805-T-A

52944889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115103195-G-A

52944889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115103195-G-T

52944910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115103174-A-G

52945006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115103079-G-C

52945006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115103079-G-T

52945018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115103067-A-T

52945050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115103035-A-G

52945084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115103000-T-C

52945133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102953-G-A

52945133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102953-G-T

52945182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102918-A-G

52945182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102918-A-T

52945433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102730-C-T

http://identifiers.org/hco/5/GRCh38#52947254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115102344-C-A

52947296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102298-G-A

52947296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102298-G-T

52947306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102288-G-A

52947466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102127-A-T

http://identifiers.org/hco/5/GRCh38#52947467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115102126-C-A

52947480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102113-T-C

http://identifiers.org/hco/5/GRCh38#52947531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115102062-A-C

52947531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102062-A-G

52947531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102062-A-T

52947533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102060-A-G

52947533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102060-A-T

52947606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115102012-A-G

52947875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115101731-A-T

52947952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115101657-A-G

52947994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115101619-T-G

52948117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115101489-G-T

http://identifiers.org/hco/5/GRCh38#52948433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115101214-A-C

52948779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115100912-G-C

52949024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115100666-A-T

52949098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115100609-T-C

52950542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115099111-T-C

52950605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115099046-C-G

52950628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115099036-C-G

52950744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115098934-T-C

52950753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115098925-A-G

52950999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115098723-G-A

http://identifiers.org/hco/5/GRCh38#52951005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115098717-A-C

52951005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115098717-A-G

52951005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115098717-A-T

52951148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115098587-T-C

http://identifiers.org/hco/5/GRCh38#52951550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115097161-A-C

52951612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115097106-G-A

52952277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115096801-T-A

52952277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115096801-T-C

52952365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115096710-T-C

52952468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115096607-A-G

http://identifiers.org/hco/5/GRCh38#52952525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115096550-A-C

http://identifiers.org/hco/5/GRCh38#52952599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115096461-A-C

http://identifiers.org/hco/5/GRCh38#52952609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115096451-C-A

http://identifiers.org/hco/5/GRCh38#52952641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115096420-A-C

52952810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115096246-C-G

52952828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115096228-T-C

52952857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115096211-T-C

http://identifiers.org/hco/5/GRCh38#52952907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115096161-A-C

http://identifiers.org/hco/5/GRCh38#52952987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115096085-C-A

52952987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115096085-C-G

http://identifiers.org/hco/5/GRCh38#52953019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115096055-C-A

52953275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115095763-G-T

52953322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115095718-G-A

52953457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115095589-T-G

52953568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115095486-G-T

http://identifiers.org/hco/5/GRCh38#52953655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115095403-A-C

52953772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115095294-T-C

http://identifiers.org/hco/5/GRCh38#52953822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115095244-A-C

52953966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115095105-T-C

http://identifiers.org/hco/5/GRCh38#52954127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115094990-C-A

52954127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115094990-C-G

52954127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115094990-C-T

52954144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115094973-G-T

52954257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115094878-G-C

52954295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115094841-G-A

52954409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115094724-G-T

52954418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115094715-A-G

52954439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115094693-G-A

52954440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115094692-G-A

52954490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115094642-G-T

http://identifiers.org/hco/5/GRCh38#52954551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115094577-C-A

52955046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115094107-T-A

52955053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115094100-A-G

52955073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115094084-G-A

52955105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115094052-G-A

52955177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115093986-C-T

52955326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115093846-G-A

52955326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115093846-G-T

52955363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115093809-A-T

52955421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115093784-A-G

http://identifiers.org/hco/5/GRCh38#52955424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115093781-C-A

52955435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115093772-A-T

52955442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115093765-G-A

52955516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115093691-C-T

52956024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092879-G-A

52956024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092879-G-T

52956118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092786-T-C

52956134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092761-A-G

52956134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092761-A-T

http://identifiers.org/hco/5/GRCh38#52956188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115092716-C-A

52956220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092686-T-A

52956277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092631-T-C

52956293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092602-G-T

52956362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092514-T-C

http://identifiers.org/hco/5/GRCh38#52956365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115092511-A-C

52956365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092511-A-G

52956408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092467-A-G

52956410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092465-G-A

52956410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092465-G-C

52956620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092264-T-C

52956742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092138-A-G

52957072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115091678-G-A

52957072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115091678-G-T

52957080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115091670-A-T

http://identifiers.org/hco/5/GRCh38#52957149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115091603-C-A

http://identifiers.org/hco/5/GRCh38#52957229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115091526-C-A

52957240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115091515-A-G

52957283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115091471-G-A

http://identifiers.org/hco/5/GRCh38#52957533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115091236-C-A

52957545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115091224-T-C

52957578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115091196-G-A

52957578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115091196-G-T

52957614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115091166-T-A

52957614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115091166-T-C

http://identifiers.org/hco/5/GRCh38#52957616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115091164-C-A

52957706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115091092-G-T

52957719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115091079-G-A

52957719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115091079-G-T

52957720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115091078-A-G

52957823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115090982-A-G

52958054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115090763-A-G

http://identifiers.org/hco/5/GRCh38#52958160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115090644-C-A

52958160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115090644-C-T

http://identifiers.org/hco/5/GRCh38#52958235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115090594-A-C

52958235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115090594-A-T

52958290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115090548-T-A

52958322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115090516-A-G

52958358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115090480-T-C

52958502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115090362-T-A

52958508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115090356-C-G

52958632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115090248-T-G

52958691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115090189-T-C

52958731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115090128-A-G

52958757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115090099-T-G

52958869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115089980-T-A

52959273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115089611-A-T

52959300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115089589-G-T

52960188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088360-T-C

52960338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088243-T-C

52960356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088225-C-T

52960429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088164-A-G

52960444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088149-C-T

52960522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088078-G-T

52960605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088005-A-G

52960609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088001-T-A

52960609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088001-T-C

52960662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087953-G-T

http://identifiers.org/hco/5/GRCh38#52960694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#115087917-C-A

52960955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087667-T-C

52960964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087658-C-T

52960977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087651-T-A

52960989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087639-A-G

52961126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087533-T-C

52961159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087508-A-G

52961238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087438-G-A

52961455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086080-T-C

52961511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086019-G-A

52979714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085812-G-C

52979735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085791-C-T

52979897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085661-G-A

52979918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085594-T-G

52979938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085574-A-T

52980062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085450-C-G

52980150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085364-C-T

http://identifiers.org/hco/5/GRCh38#52980211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#115085303-A-C

52980262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085250-G-A

http://identifiers.org/hco/5/GRCh38#52980283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#115085229-C-A

52980545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085043-C-T

52981036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115084640-T-C

52981407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115081763-C-G

52981571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115081639-C-T

52981594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115081620-C-G

52982988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115079779-T-A

52983788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078427-G-C

52983887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078326-G-C

52984036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078196-C-G

52984036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078196-C-T

52984288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115077950-G-A

52984288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115077950-G-C

52984472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115077780-A-T

52984508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115077748-T-G

52987096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115071093-C-T

52987234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115070953-T-C

52987461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115070669-T-A

52987595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115070539-C-T

52987654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115070476-G-A

52987872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115070275-G-A

52988143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115069910-T-A

http://identifiers.org/hco/5/GRCh38#52988196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115069794-C-A

52988196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 115069794-C-T

52988197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 115069793-T-C

http://identifiers.org/hco/5/GRCh38#52988211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115069779-C-A

52988214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 115069776-T-A

52988274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 115069719-G-A

52988274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 115069719-G-T

52988309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115069692-C-G

http://identifiers.org/hco/5/GRCh38#52988345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#115069662-C-A

52988345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115069662-C-G

52988345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115069662-C-T

52988386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115069622-A-G

52988578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115069268-G-A

52988908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115068978-C-G

52989016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115068888-G-A

52989109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115068801-G-A

52989145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115068765-G-A

52989154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115068763-C-T

52989219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115068700-G-A

52989219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115068700-G-T

http://identifiers.org/hco/5/GRCh38#52989404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115068523-C-A

52989483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115068453-G-C

52989553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115068383-G-A

52989553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115068383-G-C

52989603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115068334-A-G

52989604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115068333-T-C

http://identifiers.org/hco/5/GRCh38#52989644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115068297-A-C

52989644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115068297-A-G

52989707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115068194-C-T

52989896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115068049-C-T

52989962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115067983-T-C

52989962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115067983-T-G

http://identifiers.org/hco/5/GRCh38#52989963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115067982-C-A

52989963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115067982-C-T

52989985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115067959-G-A

52989985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115067959-G-T

52989990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115067954-C-T

52990010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115067943-T-C

52990010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115067943-T-G

http://identifiers.org/hco/5/GRCh38#52990058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115067904-C-A

http://identifiers.org/hco/5/GRCh38#52990262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#115067723-A-C

52990262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115067723-A-G