54846851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93021035-A-G

54846858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93021042-G-A

54846861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93021045-G-A

54847007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93021189-T-C

54847335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93021516-T-A

54847335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93021516-T-G

http://identifiers.org/hco/16/GRCh38#54847447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#93021586-C-A

54847644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93021733-T-C

54847821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93021885-G-T

54847895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93021952-G-T

http://identifiers.org/hco/16/GRCh38#54847927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93021982-A-C

54848425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93023208-A-G

54848507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93023276-C-T

54848513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93023280-G-A

http://identifiers.org/hco/16/GRCh38#54848527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93023294-C-A

54848545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93023312-C-T

54848558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93023325-G-A

http://identifiers.org/hco/16/GRCh38#54848565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93023332-C-A

54848596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93023363-G-A

54848596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93023363-G-T

54848640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93023388-G-T

54848792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93023522-A-T

http://identifiers.org/hco/16/GRCh38#54848828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93023559-C-A

http://identifiers.org/hco/16/GRCh38#54848923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93023643-C-A

54849125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93023835-C-T

54849167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93023881-G-A

54849167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93023881-G-C

http://identifiers.org/hco/16/GRCh38#54849221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93023938-C-A

54849221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93023938-C-T

http://identifiers.org/hco/16/GRCh38#54849238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93023955-C-A

http://identifiers.org/hco/16/GRCh38#54849336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93024053-C-A

54849358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93024075-G-C

54849358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93024075-G-T

54849460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93024171-A-G

54849581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93024283-G-T

54851617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93025294-T-G

54851736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93025393-G-A

54851736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93025393-G-T

54851845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93025499-G-A

54851845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93025499-G-T

54851964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93025618-G-T

54852074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93025733-A-G

54854118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93024407-T-G

54854611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93026751-A-G

54855009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93027109-A-G

54855034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93027133-G-A

54855107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93027206-A-T

54855219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93027316-T-C

54855287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93027353-T-A

54855352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93027396-T-A

54855352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93027396-T-C

54855466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93027483-A-G

54855467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93027484-G-A

http://identifiers.org/hco/16/GRCh38#54855516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93027540-A-C

54855594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93027615-G-T

54856458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93030422-A-G

54856458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93030422-A-T

54862074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93038373-G-T

54862078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93038377-C-T

http://identifiers.org/hco/16/GRCh38#54862487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93038816-C-A

54862487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93038816-C-T

54862543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93038868-C-T

54863012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93039321-G-A

54863049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93039358-G-A

http://identifiers.org/hco/16/GRCh38#54863484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93039788-C-A

54863491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93039795-C-T

54863848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93040247-T-G

54863906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93040305-C-T

54863987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93040384-A-G

54865440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93041487-C-T

http://identifiers.org/hco/16/GRCh38#54865687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93041711-A-C

54865695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93041719-A-G

54865696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93041720-A-G

54866776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042002-G-A

54867390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042301-G-T

54867415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042326-G-A

http://identifiers.org/hco/16/GRCh38#54867749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93042564-A-C

54867778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042593-G-A

54867812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042635-A-T

54867818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042641-C-G

54868414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93043798-A-G

54868465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93043856-G-A

54870236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045996-A-G

54870363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046124-T-C

54870365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046126-G-A

54871959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046896-G-A

54872060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93047009-T-C

54872881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93047666-C-T

54873319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93048062-A-G

54873413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93048154-C-T

http://identifiers.org/hco/16/GRCh38#54873438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93048169-C-A

54873486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93048215-C-T

http://identifiers.org/hco/16/GRCh38#54873907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93048533-A-C

54875246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93049715-G-A

54875254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93049723-T-A

54875259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93049728-T-C

54875548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93050005-C-T

54875629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93050082-T-C

54875747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93050171-A-T

54875909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93050323-G-T

http://identifiers.org/hco/16/GRCh38#54876012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93050397-C-A

54876012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93050397-C-T

54876293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93050617-T-C

http://identifiers.org/hco/16/GRCh38#54876315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93050638-C-A

54876315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93050638-C-T

54878300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93051878-C-T

54878313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93051887-A-G

54878488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93052052-G-T

54878676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93052199-C-G

54878906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93052359-C-T

54878958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93052404-A-G

54879084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93052986-G-A

54879103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053008-T-C

54879347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053201-G-A

54879360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053218-T-A

54879468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053310-T-C

http://identifiers.org/hco/16/GRCh38#54879798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93053597-C-A

54879862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053663-G-A

54879894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053695-C-T

54880066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053866-T-C

54881882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93055299-T-C

54885387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93057815-A-G

54885425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93057873-G-A

54885511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93057952-G-A

54885696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058149-T-G

54885718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058171-G-A

54885718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058171-G-C

http://identifiers.org/hco/16/GRCh38#54885766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93058218-A-C

54890108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93061442-G-A

54890108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93061442-G-T

54890516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93061848-T-C

54890604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93061936-C-T

54890998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93062327-G-A

54891130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93062455-T-C

54891385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93062722-G-T

54891462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93062790-G-T

54891478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93062816-G-T

http://identifiers.org/hco/16/GRCh38#54891519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93062856-C-A

54891572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93062907-G-T

54891635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93062969-G-T

54891665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93062999-G-A

54892761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063970-G-A

54892774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063983-C-T

54892918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93064061-G-A

54893084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93064199-G-T

54893209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93064304-G-A

54893209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93064304-G-T

http://identifiers.org/hco/16/GRCh38#54893224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93064317-C-A

54893224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93064317-C-T

http://identifiers.org/hco/16/GRCh38#54893301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93064394-C-A

54893327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93064420-A-G

54893433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93064523-C-T

54893465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93064554-A-G

http://identifiers.org/hco/16/GRCh38#54893577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93064653-C-A

54893577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93064653-C-T

54893654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93064724-T-G

54893659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93064729-A-G

54894274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93065044-T-G

54894320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93065097-G-A

54894553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93065270-G-A

54894553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93065270-G-C

54894929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93065585-G-A

54909492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93068825-A-G

54909762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93069050-T-C

54914546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93069715-T-C

54914548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93069717-T-C

54914604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93069792-C-T

54916898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93070997-C-T

54917253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93071416-T-A

54917445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93071585-A-T

54917506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93071645-A-G

54917546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93071672-A-G

54918092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93072164-G-A

54918092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93072164-G-T

54918364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93072701-T-C

54918461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93072857-T-C

54918502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93072894-T-C

54918520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93072911-C-T

54918668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93073043-T-C

54918902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93073259-C-T

54919004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93073370-C-T

54920101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93073973-G-A

54920207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93074080-T-A

54920450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93074302-T-C

54920732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93074559-A-G

54920753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93074579-A-G

54920920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93074740-A-T

54921654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93075442-A-G

54921655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93075443-A-G

54921743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93075531-A-G

54922156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93075988-T-C

54922156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93075988-T-G

54922160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93075992-A-T

54922266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93076101-A-G

http://identifiers.org/hco/16/GRCh38#54922704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93076467-A-C

54922800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93076555-G-A

54923081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93076811-C-T

54923190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93076917-A-G

54923245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93076971-T-C

http://identifiers.org/hco/16/GRCh38#54923312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93077034-C-A

http://identifiers.org/hco/16/GRCh38#54923334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93077056-C-A

http://identifiers.org/hco/16/GRCh38#54923407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93077129-C-A

54923407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93077129-C-G

54923407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93077129-C-T

54923602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non coding transcript exon variant
orthologous variants: 93077336-C-T

54923615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non coding transcript exon variant
orthologous variants: 93077349-T-C

54923616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non coding transcript exon variant
orthologous variants: 93077350-A-G

54923646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non coding transcript exon variant
orthologous variants: 93077378-A-G

54923755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93077486-A-G

54924024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93077817-T-C

http://identifiers.org/hco/16/GRCh38#54924076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93077881-C-A

54924343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93078118-T-A

54924348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93078123-T-C

54924355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93078132-G-C

http://identifiers.org/hco/16/GRCh38#54924371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93078148-A-C

54924437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93078216-A-G

54924437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93078216-A-T

54924697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93078468-T-C

54925130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non coding transcript exon variant
orthologous variants: 93078967-C-T

54925350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93079189-A-G

54925444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93079283-A-G

54925519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93079358-G-C

54925552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93079390-G-T

54925657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93079494-G-A

54925671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93079508-G-T

54925855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93079672-T-C

54927101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93080902-A-G

54927168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93080974-G-C

54927349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93081154-C-T

54927390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93081195-G-A

http://identifiers.org/hco/16/GRCh38#54927442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93081247-A-C

54927442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93081247-A-T

54927598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93081403-G-T

54927600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93081405-G-C

54927600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93081405-G-T

54927633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93081438-T-A

54927848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93081624-G-C

54928293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93082108-T-G

54928340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082140-T-A

54928340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082140-T-G

http://identifiers.org/hco/16/GRCh38#54928345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93082145-A-C

54928349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082149-T-G

http://identifiers.org/hco/16/GRCh38#54928370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93082168-A-C

http://identifiers.org/hco/16/GRCh38#54928425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93082247-C-A

54928425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082247-C-G

54928469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082291-G-A

54928469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082291-G-C

54928469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082291-G-T

http://identifiers.org/hco/16/GRCh38#54928927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93082557-C-A

54928927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non coding transcript exon variant
orthologous variants: 93082557-C-T

54928977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 93082606-G-A

54928977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 93082606-G-T

54929022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 93082637-G-A

54929022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 93082637-G-T

54929066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non coding transcript exon variant
orthologous variants: 93082680-G-A

54929066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non coding transcript exon variant
orthologous variants: 93082680-G-T

http://identifiers.org/hco/16/GRCh38#54929087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#93082701-C-A

54929087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37078
most severe consequence: non coding transcript exon variant
orthologous variants: 93082701-C-T