http://identifiers.org/hco/2/GRCh38#64631860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20602796-C-A

http://identifiers.org/hco/2/GRCh38#64632219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20602459-A-C

64632219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20602459-A-G

64632455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20602253-A-G

64632538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20602172-T-G

64632549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20602163-T-A

64632550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20602162-C-T

http://identifiers.org/hco/2/GRCh38#64632831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20601864-C-A

64632831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20601864-C-T

http://identifiers.org/hco/2/GRCh38#64632925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20601775-C-A

64632967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20601737-C-T

http://identifiers.org/hco/2/GRCh38#64633022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20601701-C-A

64633022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20601701-C-T

64633517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20601232-C-T

64633606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20601143-T-A

64633606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20601143-T-C

64633630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20601119-T-C

64633768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20600987-A-G

64633775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20600981-T-C

64633777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20600979-G-A

64633777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20600979-G-T

http://identifiers.org/hco/2/GRCh38#64634214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20600574-A-C

64634257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20600532-A-G

64634310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20600477-T-A

64634564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20600229-G-A

64634564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20600229-G-T

64634909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20599727-G-T

http://identifiers.org/hco/2/GRCh38#64634945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20599693-C-A

64634945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20599693-C-T

http://identifiers.org/hco/2/GRCh38#64634974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20599650-C-A

http://identifiers.org/hco/2/GRCh38#64634975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20599649-C-A

64635023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20599600-T-C

64635740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20598917-T-A

64635740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20598917-T-G

64635890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20598769-G-T

64635896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20598763-T-C

64635911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20598748-G-A

64635911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3 prime UTR variant
orthologous variants: 20598748-G-T

64636225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: missense variant
orthologous variants: 20598435-G-A

64636248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: synonymous variant
orthologous variants: 20598412-G-A

64636248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: synonymous variant
orthologous variants: 20598412-G-C

64636455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: synonymous variant
orthologous variants: 20598202-G-A

64636509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: synonymous variant
orthologous variants: 20598145-T-C

64636579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 20598096-T-A

http://identifiers.org/hco/2/GRCh38#64636919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20597756-C-A

http://identifiers.org/hco/2/GRCh38#64636929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20597746-C-A

64637292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20597439-T-C

64637292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20597439-T-G

64637306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20597425-A-T

64637508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20597256-C-T

64637549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20597237-T-C

64638276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20596535-T-C

64638675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20596217-C-T

64640294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20595228-C-T

64640854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20594758-G-A

64641380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20594126-C-T

64641793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20593868-G-A

64642131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20593601-A-G

64642525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20593044-A-G

64642905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20592756-G-A

64642905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20592756-G-T

64644303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20590769-T-C

http://identifiers.org/hco/2/GRCh38#64644645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20590539-C-A

64644704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20590488-A-G

http://identifiers.org/hco/2/GRCh38#64644773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20590422-C-A

64644773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20590422-C-T

64644841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20590368-G-T

http://identifiers.org/hco/2/GRCh38#64644882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20590332-C-A

64644937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20590284-G-A

64644937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20590284-G-T

64645147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20590087-T-C

64645564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20589793-T-C

64645778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20589577-T-C

http://identifiers.org/hco/2/GRCh38#64646248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20589297-C-A

64646475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20589071-A-G

64646489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 20589057-T-C

64646523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 20589030-G-T

http://identifiers.org/hco/2/GRCh38#64646553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20589007-C-A

64646554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20589006-T-C

64647007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20588609-T-C

http://identifiers.org/hco/2/GRCh38#64647337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20588296-A-C

64647337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20588296-A-G

64648318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20587382-T-C

64648347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20587348-A-T

64648721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20586845-G-A

64649099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20586476-G-A

64649127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20586418-C-T

http://identifiers.org/hco/2/GRCh38#64649133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20586412-C-A

64649133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20586412-C-T

64649826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585808-G-A

64650411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585443-C-T

64650466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585388-A-T

64650702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585135-T-C

64650743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20585094-T-C

64651201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20584500-C-T

64651433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20584254-T-A

64651538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20584155-T-A

64651538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20584155-T-C

http://identifiers.org/hco/2/GRCh38#64651952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20583782-C-A

64651952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20583782-C-T

64652139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20583579-G-A

64652278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20583473-G-A

64652475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20583317-G-A

64652581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20583208-A-G

64652786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20583024-T-A

64652854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582963-T-C

64653035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582777-G-A

64653035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582777-G-T

64653051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582761-T-A

64653103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582713-G-A

64653103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582713-G-T

64653580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582305-G-A

64653580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582305-G-T

http://identifiers.org/hco/2/GRCh38#64653582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20582303-C-A

64653582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582303-C-T

http://identifiers.org/hco/2/GRCh38#64653593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20582294-C-A

64653593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20582294-C-T

http://identifiers.org/hco/2/GRCh38#64653604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#20582283-C-A

64653604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20582283-C-T

64653679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20582213-T-C

64653692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20582200-T-A

64653692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20582200-T-C

64653692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20582200-T-G

64653698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20582194-G-A

64653742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20582160-G-A

64653742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20582160-G-T

64653880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20582029-G-A

64653880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20582029-G-C

64653880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20582029-G-T

64654041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20581865-G-A

64654041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20581865-G-T

64654077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20581841-G-A

64654077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20581841-G-C

64654284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 20581581-C-T

64654663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 20581328-G-T

64655119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20580866-A-T

64655301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20580509-C-G

64655472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20580365-T-C

64655744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20580126-C-T

64655822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20580052-A-G

64656940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20578965-C-T

64657666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20578218-A-T

64657857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20578009-C-T

64658668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20577144-T-C

64658668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20577144-T-G

64659205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20576988-G-A

64659205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20576988-G-T

64659552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20576681-T-C

64659557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20576676-A-G

http://identifiers.org/hco/2/GRCh38#64659573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20576662-A-C

64659594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20576641-T-C

64660566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20572234-T-C

64660566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20572234-T-G

http://identifiers.org/hco/2/GRCh38#64660779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20571876-A-C

64666512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20567530-G-T

64666730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20566949-A-G

64667319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20566195-C-T

http://identifiers.org/hco/2/GRCh38#64667409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#20566106-A-C

64667409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20566106-A-T

http://identifiers.org/hco/2/GRCh38#64667505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20566010-A-C

64667597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20565332-G-A

64668080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20564916-A-G

64668149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20564855-T-C

64668903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20564220-A-G

64669625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20563301-G-C

64669854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20562699-T-A

64669854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20562699-T-G

http://identifiers.org/hco/2/GRCh38#64670233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20562076-A-C

64674831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20559564-T-G

http://identifiers.org/hco/2/GRCh38#64674874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20559527-C-A

64674898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20559502-T-C

64675063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20559336-T-C

64675253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20559190-A-T

64675423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20559088-T-C

64675712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20558919-A-G

64675712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20558919-A-T

64675964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20558672-T-C

64675991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20558645-C-T

64676169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20558513-G-A

64676201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20558487-T-A

64676387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20558328-C-T

64676574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20558078-G-C

64676581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20558071-T-C

http://identifiers.org/hco/2/GRCh38#64676693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20557970-C-A

http://identifiers.org/hco/2/GRCh38#64676872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20557832-A-C

64676872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20557832-A-G

64677395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20557011-A-G

64677604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20556053-A-G

64677627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20556030-G-C

64678298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20555571-C-T

64678361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20555510-G-A

64678393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20555473-A-G

64678490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20555383-T-C

64678590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20554836-G-C

64678621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20554813-T-A

64678684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20554754-T-C

64678725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20554717-T-A

64678794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20554661-T-A

64679434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20554047-C-T

64679525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20553979-C-G

64679525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20553979-C-T

http://identifiers.org/hco/2/GRCh38#64679583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20553926-A-C

64679755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20553751-G-C

64680373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20553094-A-G

http://identifiers.org/hco/2/GRCh38#64680753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20552629-A-C

64681405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20552148-A-G

64681418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20552135-G-C

64681634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20551785-C-T

http://identifiers.org/hco/2/GRCh38#64681704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20551724-A-C

64681704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20551724-A-G

64687505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20545350-A-G

64687879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20545023-A-G

64688491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20544747-C-T

64689186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20544213-G-A

64689427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20544028-A-T

http://identifiers.org/hco/2/GRCh38#64696689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20537953-C-A

64696689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20537953-C-T

http://identifiers.org/hco/2/GRCh38#64696886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20537771-A-C

64697305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20536990-A-G

64697404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20536894-A-G

64697644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20536713-G-A

64697644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20536713-G-C

64697814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20536579-G-A

64697945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20536452-A-G

http://identifiers.org/hco/2/GRCh38#64698021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20536384-C-A

64698218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20536167-T-G

64698271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20536123-T-C

64698567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20535781-C-T

64699201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20535217-G-A

64699372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20535053-A-T

64700388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20534494-T-G

64700563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20534325-T-C

64701172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20533976-G-T

64701486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20533664-G-A

64701486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20533664-G-C

http://identifiers.org/hco/2/GRCh38#64702292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20531782-C-A

64702292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20531782-C-G

64702473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20531616-T-C

64702497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20531592-A-G

64702642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20531434-T-C

64702642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20531434-T-G

64702771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20531306-A-G

http://identifiers.org/hco/2/GRCh38#64703127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20530948-C-A

64703131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20530944-G-A

64705052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20530516-A-G

64705194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20530391-T-A

64705615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20529401-T-A

64705776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20529316-C-T

64705906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20529208-T-G

64705921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20529193-T-C

http://identifiers.org/hco/2/GRCh38#64706022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20529135-C-A

64706022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20529135-C-G

64706037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20529122-A-G

64706143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20529016-G-A

64708242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20528434-C-T

http://identifiers.org/hco/2/GRCh38#64709092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20527395-A-C

64709092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20527395-A-G

64709112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20527377-T-C

64709143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20527346-C-G

64710552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20526916-T-C

64710552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20526916-T-G

http://identifiers.org/hco/2/GRCh38#64710716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20526712-A-C

64710716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20526712-A-T

64711256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20526489-G-A

64711357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20526388-A-G

64711539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20526191-G-A

http://identifiers.org/hco/2/GRCh38#64711572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20526158-C-A

64711762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20525966-A-G

64711946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20525787-G-T

64712296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20524310-T-C

64712512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20523889-A-G

64712582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20523817-G-A

64712582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20523817-G-C

64712628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20523774-A-T

64713224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20523483-C-T

64713286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20523432-T-A

64713414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20523313-A-G

64715565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20522725-A-G

64716071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20522264-T-A

64716725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20521512-A-G

http://identifiers.org/hco/2/GRCh38#64716885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20521316-A-C

64717164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20520818-T-C

64717407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20520610-G-C

64717675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20520429-C-T

64718303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20519886-G-A

64718552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20519523-C-T

64718637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20519421-C-G

64718685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20519383-A-G

64718778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20519294-T-C

64724086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20515336-G-A

64724086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20515336-G-C

64724089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20515333-C-T

64724123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20515293-C-T

64724264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20515163-T-G

http://identifiers.org/hco/2/GRCh38#64724393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20515034-A-C

64724405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20515022-T-C

64724407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20515020-G-C

64724577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20514859-C-T

64724616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20514825-A-G

64724807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20514427-T-C

64725588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20513337-T-C

64726031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20513189-T-A

64726031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20513189-T-C

64726244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20513026-C-T

64726517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20512881-A-G

64727933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20511757-G-A

64728251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20511503-T-C

64728349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20511444-T-A

64728863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20511272-C-T

64728892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20511233-G-A

64728892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20511233-G-C

64728892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20511233-G-T

64728899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20511226-C-T

64728914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20511212-C-T

64729605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20510660-A-G

64730146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20509910-T-C

64730814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20509735-C-G

64730814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20509735-C-T

64730898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20509668-C-G

64731620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20508975-G-A

64731632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20508963-G-A

64731864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20508746-C-T

64731939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20508672-G-A

64732138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20508481-T-C

64732257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20508397-C-T

64732258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20508396-G-A

64732264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20508390-C-T

64732321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20508374-T-C

64732355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20508340-G-A

64732635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20507499-T-A

64733185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20507226-G-A

64733185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20507226-G-T

64733405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20507099-G-C

64733426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20507069-G-A

64738138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20506860-A-T

64738185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20506818-T-C

64738233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20506786-A-G

64738298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20506719-G-A

64738398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20506491-C-G

64738582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20506283-T-C

64739696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20505214-G-C

64739921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20504985-T-A

64739921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20504985-T-C

64740746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20504732-A-G

64741616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20503694-T-C

64741637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20503673-G-A

64742399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20503267-C-T

64742420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20503246-T-C

64742469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20503193-T-C

64742647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20503029-T-C

64742684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20503009-T-C

64742692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20503002-T-C

64742692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20503002-T-G

64743034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20502634-G-T

64743208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20502463-A-G

64744177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20501197-T-C

64744177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20501197-T-G

64745001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20499581-G-A

64745130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20499455-G-A

64746376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20498297-A-G

64746818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20497891-A-T

http://identifiers.org/hco/2/GRCh38#64746887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20497836-C-A

64746887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20497836-C-T

64746924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20497801-T-C

64746967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20497758-A-G

64747034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20497688-G-A

http://identifiers.org/hco/2/GRCh38#64747305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20497372-A-C

64747305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20497372-A-G

64747330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20497346-T-G

64747526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20497210-G-T

http://identifiers.org/hco/2/GRCh38#64747639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#20497120-A-C

http://identifiers.org/hco/2/GRCh38#64748803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20495189-C-A

64748803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20495189-C-T

64748876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20495123-A-G

64749423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20494588-T-C

http://identifiers.org/hco/2/GRCh38#64749643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20494394-A-C

64750227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20493827-A-G

64750389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non coding transcript exon variant
orthologous variants: 20493672-T-C

64750398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non coding transcript exon variant
orthologous variants: 20493663-G-T

64750412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non coding transcript exon variant
orthologous variants: 20493649-T-C

64750412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non coding transcript exon variant
orthologous variants: 20493649-T-G

64750584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non coding transcript exon variant
orthologous variants: 20493532-T-C

64750656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non coding transcript exon variant
orthologous variants: 20493467-A-G

64750762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non coding transcript exon variant
orthologous variants: 20493379-A-G

64750767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non coding transcript exon variant
orthologous variants: 20493374-G-A

64750841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non coding transcript exon variant
orthologous variants: 20493310-G-C

64750930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 20493238-G-A

http://identifiers.org/hco/2/GRCh38#64750991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#20493177-C-A

64750991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non coding transcript exon variant
orthologous variants: 20493177-C-T

64751004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 20493165-G-A

64751004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 20493165-G-C

64751004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30784
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 20493165-G-T