74776502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 5 prime UTR variant
orthologous variants: 115078340-A-G

74776626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078445-C-T

http://identifiers.org/hco/17/GRCh38#74776692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115078503-A-C

74776692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078503-A-G

74776706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078517-G-A

http://identifiers.org/hco/17/GRCh38#74776744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115078556-C-A

74777138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078910-G-A

74777138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078910-G-T

74777139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078911-T-G

74777223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078992-T-C

http://identifiers.org/hco/17/GRCh38#74777224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115078993-C-A

74777224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078993-C-T

74777266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_acceptor_variant, splice_region_variant
orthologous variants: 115079038-G-A

74777290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115079062-C-T

74777354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115079127-C-G

74777354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115079127-C-T

74777442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115079217-T-A

http://identifiers.org/hco/17/GRCh38#74777482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115079257-C-A

74777977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115079669-A-G

74777977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115079669-A-T

74778187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115079878-G-A

74778424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115080114-T-G

http://identifiers.org/hco/17/GRCh38#74779242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115080438-A-C

74779242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115080438-A-G

74779411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115080598-C-G

74779455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115080642-G-A

74779518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115080695-T-C

74780243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115082934-A-G

74780330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115083013-T-C

http://identifiers.org/hco/17/GRCh38#74780406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115083067-C-A

74780451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115083084-A-G

74780482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115083110-C-T

74780701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115083283-A-G

74780706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115083288-C-T

74785064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087745-C-T

74785138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087792-A-G

74785215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087835-C-T

74785222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087842-G-A

74785401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088000-C-T

74785405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088004-A-T

74785411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088010-G-A

74785411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088010-G-T

74785446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088026-A-G

74785446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088026-A-T

74785453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088033-G-T

74785454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088034-G-A

74785454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088034-G-C

74785523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115088103-C-T

74785556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115088136-C-T

74785574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115088154-C-T

74785584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115088164-G-C

74785598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115088178-C-T

http://identifiers.org/hco/17/GRCh38#74785626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115088231-C-A

74785626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115088231-C-G

74785626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115088231-C-T

http://identifiers.org/hco/17/GRCh38#74785672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115088277-C-A

74785672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115088277-C-G

74785672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115088277-C-T

74785673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115088278-G-A

74785673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115088278-G-T

74785722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115088343-G-A

74785722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115088343-G-T

74785747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115088369-A-G

http://identifiers.org/hco/17/GRCh38#74785750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115088372-C-A

74785750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115088372-C-T

http://identifiers.org/hco/17/GRCh38#74785768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115088390-C-A

74785768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115088390-C-G

74785832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115088479-T-C

74785973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115088612-A-G

74786052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115088680-A-G

74786069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115088721-C-T

74786108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115088794-G-A

74786160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115088856-C-T

74786577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115089561-A-G

74786603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115089601-G-T

74786647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115089649-G-A

74786652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115089686-C-T

74786840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115089928-C-G

74786942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115090015-A-T

74787005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115090077-A-G

74788679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115091559-G-A

74788700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115091584-G-A

74788700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115091584-G-T

74788705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115091589-G-T

http://identifiers.org/hco/17/GRCh38#74788784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115091641-C-A

74788784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 115091641-C-G

74788784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 115091641-C-T

74788810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115091667-G-A

74788810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115091667-G-T

74788916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115091787-G-A

74788928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115091797-G-A

74788928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115091797-G-T

http://identifiers.org/hco/17/GRCh38#74788942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115091818-C-A

http://identifiers.org/hco/17/GRCh38#74788983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115091852-C-A

74788983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115091852-C-T

74789072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115091931-C-T

74789267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115092083-C-T

74790202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 115092144-G-A

http://identifiers.org/hco/17/GRCh38#74790334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115092255-C-A

74790334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115092255-C-T

http://identifiers.org/hco/17/GRCh38#74790364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115092285-A-C

74790371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115092292-T-A

74790371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115092292-T-C

74790372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115092293-G-A

74790372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115092293-G-T

74790375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115092296-G-A

74790375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115092296-G-T

74790697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115092556-C-T

http://identifiers.org/hco/17/GRCh38#74790756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115092604-C-A

74790757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115092605-A-T

http://identifiers.org/hco/17/GRCh38#74790768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115092616-C-A

74790848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115092786-G-A

74790848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115092786-G-T

http://identifiers.org/hco/17/GRCh38#74790897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115092911-C-A

74791061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115093062-T-G

74791064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115093065-G-A

74791064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115093065-G-T

http://identifiers.org/hco/17/GRCh38#74791164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115093145-C-A

74791164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115093145-C-T

74791289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115093245-C-T

74791622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, undefined
orthologous variants: 115093313-T-C

74791844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, undefined
orthologous variants: 115093530-G-A

74792620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115093693-C-T

74792705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115093770-A-G

74793019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115094112-G-A

74793310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115094494-T-C

http://identifiers.org/hco/17/GRCh38#74793414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115094612-C-A

74793818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115095026-G-T

74793823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115095031-T-C

74793946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115095180-A-G

74793995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115095228-C-T

74794090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115095310-T-A

74794855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115095735-C-G

74794894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115095779-G-A

74794957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115095832-A-G

74794957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115095832-A-T

74794963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115095837-T-A

74794963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115095837-T-C

74794963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115095837-T-G

http://identifiers.org/hco/17/GRCh38#74794969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115095843-C-A

74794969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115095843-C-G

74794969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115095843-C-T

http://identifiers.org/hco/17/GRCh38#74795082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115095958-C-A

74795082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: synonymous variant
orthologous variants: 115095958-C-T

74795127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096008-G-A

74795127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096008-G-C

74795151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096032-G-A

74795187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096048-G-A

74795214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096082-T-C

74795241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096108-G-A

74795241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096108-G-T

74795355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096185-G-A

74795420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096236-T-C

74795420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096236-T-G

http://identifiers.org/hco/17/GRCh38#74795434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115096242-C-A

74795434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096242-C-T

74795437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096245-G-A

74795437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096245-G-T

http://identifiers.org/hco/17/GRCh38#74795463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115096255-C-A

74795463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096255-C-T

74795548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: synonymous variant
orthologous variants: 115096325-C-T

74795575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: missense variant
orthologous variants: 115096352-T-A

74795575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: synonymous variant
orthologous variants: 115096352-T-C

http://identifiers.org/hco/17/GRCh38#74795672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115096448-C-A

74795672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096448-C-T

http://identifiers.org/hco/17/GRCh38#74795689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115096465-A-C

74795689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096465-A-G

74795882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115096596-G-A

74796425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115097120-C-G

74796541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115097240-G-A

74797025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115097647-T-G

74797203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115097827-G-T

74797219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115097843-A-G

74797315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115097937-G-A

74797315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115097937-G-T

74797317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115097939-G-A

74797349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115097971-G-A

http://identifiers.org/hco/17/GRCh38#74797380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115098001-A-C

74797440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115098070-G-A

74797441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115098071-G-A

74797942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115098494-C-T

74797945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115098497-T-C

http://identifiers.org/hco/17/GRCh38#74798078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115098627-C-A

74798078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115098627-C-T

74798103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115098651-T-C

74798167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115098708-A-G

74798193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115098732-A-G

74798197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115098736-C-T

http://identifiers.org/hco/17/GRCh38#74798471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115098991-A-C

74798535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 115099009-T-G

74798703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115099135-C-T

74798932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115099501-G-T

74799013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115099571-G-A

74799046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115099593-G-A

74799055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115099602-C-T

74799355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115099851-G-A

74799393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115099889-G-C

74799536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115100019-A-G

74799576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115100054-A-G

74799744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115100182-C-G

http://identifiers.org/hco/17/GRCh38#74799876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115100310-A-C

74800401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115100875-C-T

74801134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115101345-T-C

74801297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115101463-C-T

74801320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115101486-G-A

74801320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115101486-G-C

74801329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115101495-G-A

74801329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115101495-G-C

74801340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115101506-C-T

74802004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115101970-G-T

74802013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115101987-G-A

74802102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115102085-C-G

74802226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115102228-C-T

74802258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115102260-C-T

74803067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115102709-A-G

http://identifiers.org/hco/17/GRCh38#74803159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115102769-C-A

74803162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115102772-T-C

74803252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115102860-T-G

74803386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115102984-C-G

74803695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115103271-C-T

74803702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115103278-A-G

74804021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115103890-C-T

74804086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115103941-T-G

74804099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115103954-C-G

74804474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115104681-C-T

http://identifiers.org/hco/17/GRCh38#74804667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115104858-A-C

74804796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115104953-G-A

74804911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115105062-G-A

74804911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115105062-G-T

74804924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115105071-G-A

74804932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115105085-A-G

http://identifiers.org/hco/17/GRCh38#74804963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115105116-A-C

74804963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115105116-A-G

74805395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115105720-A-G

74805931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115106188-G-A

74805993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115106248-C-T

74806022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115106267-A-G

74806103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115106336-T-G

74806152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115106384-A-G

74806391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115106531-G-A

74806480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115106607-G-A

74806492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115106619-C-T

74806635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115106774-C-T

74807583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115108202-C-T

74807858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115108490-C-T

74808210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115108842-G-A

74808589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115109150-T-A

74808630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115109204-G-C

74808728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115109274-G-A

http://identifiers.org/hco/17/GRCh38#74808732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115109278-C-A

74810360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115110415-C-T

74810401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115110448-G-A

74810428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115110467-G-T

http://identifiers.org/hco/17/GRCh38#74810449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115110488-A-C

74810449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115110488-A-G

74810545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115110584-G-C

74810566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115110596-G-C

74810586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115110617-G-A

74810599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115110634-G-A

74810600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115110635-C-T

74810670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115110697-A-G

74810796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115110783-C-G

74810837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115110824-A-T

74810913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115110898-T-C

74811018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115110998-G-A

74812475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115112926-G-A

74812647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115113097-C-T

74812674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115113125-C-G

74812707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115113159-C-T

74812721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115113173-A-G

74812723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115113174-A-G

74812764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115113218-G-A

74812858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115113308-G-A

74813037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115113443-C-G

74813177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115113563-G-A

74813914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115113734-G-T

74814605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115114202-C-G

74814669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115114251-C-T

74814736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115114328-C-T

74814747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115114339-C-T

74814753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115114345-A-G

74814777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115114376-G-A

74814804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115114402-C-T

74814835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115114433-G-A

http://identifiers.org/hco/17/GRCh38#74815129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115114784-C-A

74815200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115114845-G-A

74815234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115114876-G-A

74815605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115115191-G-T

74815624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115115210-G-A

74815755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115115310-C-T

74816151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115115873-G-A

74816183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115115905-G-A

74816323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115116037-G-A

74816332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115116046-G-A

74816539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115116253-C-T

74816645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115116356-G-A

74816717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115116426-C-T

74816877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115116580-G-A

http://identifiers.org/hco/17/GRCh38#74816969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115116662-A-C

74816969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115116662-A-G

74817223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115116852-C-T

74817257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115116885-T-C

74817308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115116935-G-T

74817322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115116949-C-T

74817632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115117160-G-A

74817659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115117187-T-C

74817700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115117239-G-A

http://identifiers.org/hco/17/GRCh38#74817712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115117249-C-A

74817750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115117278-C-T

74818056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115117547-A-G

74818150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115117644-G-A

74818150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115117644-G-T

74818419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115117898-G-A

74818650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115118135-A-G

74818672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115118158-G-A

74818735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115118228-T-C

74818847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115118336-C-T

74819207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115118728-A-G

74819218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115118742-C-T

74819229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115118753-C-T

74819490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119002-G-T

74819530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119032-G-A

http://identifiers.org/hco/17/GRCh38#74819601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115119100-A-C

74819629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119132-G-A

74819629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119132-G-T

74819720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119213-A-G

http://identifiers.org/hco/17/GRCh38#74819722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115119216-C-A

74819767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: synonymous variant
orthologous variants: 115119264-C-G

74819767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: synonymous variant
orthologous variants: 115119264-C-T

74819776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: synonymous variant
orthologous variants: 115119273-G-A

74819776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: synonymous variant
orthologous variants: 115119273-G-T

74819880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119376-T-G

http://identifiers.org/hco/17/GRCh38#74819898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115119394-C-A

74819918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119414-G-A

74819918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119414-G-T

74819934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119429-T-A

74819934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119429-T-C

74819942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119432-G-C

74819942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119432-G-T

74820128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119578-G-A

74820153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119604-A-G

74820302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119720-G-A

74820391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119822-G-A

74820517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119952-C-T

74820583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115119975-G-A

74820801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115120298-A-G

74820838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115120333-G-T

74822938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115122755-A-G

http://identifiers.org/hco/17/GRCh38#74823387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115123167-A-C

74823550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115123311-A-G

74823587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115123349-T-G

http://identifiers.org/hco/17/GRCh38#74823618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115123395-C-A

74823663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115123472-G-C

74823674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115123491-C-T

74823899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115123771-T-C

74823935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115123832-G-A

74824193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115124040-T-C

74824673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115124495-G-T

74824676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115124498-C-T

74824987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115124822-C-T

74825062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115124905-A-G

74825098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115124941-C-T

74825170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115124991-C-T

74825351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115125074-A-G

74825374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115125099-G-T

74825693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115125392-C-T

http://identifiers.org/hco/17/GRCh38#74825739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115125423-A-C

http://identifiers.org/hco/17/GRCh38#74825742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115125426-C-A

74825742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115125426-C-T

74825976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115125582-C-T

74826182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115125784-C-T

74826185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115125787-C-T

http://identifiers.org/hco/17/GRCh38#74826186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115125788-A-C

74826251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115126033-G-A

74826264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115126046-G-C

74826264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115126046-G-T

http://identifiers.org/hco/17/GRCh38#74826281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115126062-A-C

74826281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115126062-A-G

74826298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115126072-C-G

http://identifiers.org/hco/17/GRCh38#74826467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115126172-A-C

74826664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115126336-A-G

74826714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115126368-A-G

74826798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115126430-C-T

74827052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115126687-C-T

74827252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115126860-A-T

74827321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115126924-A-T

74827987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115127471-C-T

74828816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115128311-A-G

74828904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115128425-C-T

74828907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115128428-A-G

74829526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115129157-T-C

74829583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115129214-G-A

74829584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115129215-G-C

74829584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115129215-G-T

74831071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115130428-G-A

http://identifiers.org/hco/17/GRCh38#74831291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115130636-A-C

74831569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115130878-G-A

74833924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115132522-C-T

http://identifiers.org/hco/17/GRCh38#74833989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115132557-C-A

74834105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115132628-C-T

74834106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115132629-T-C

74834268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115132706-C-T

74834316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115132756-G-A

74834435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115132840-C-T

74834700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115133086-T-C

74834833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115133186-C-T

74834871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115133227-G-A

74835075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115133433-G-A

74835075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115133433-G-T

74835077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115133435-G-A

74835184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115133529-G-A

74835569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115133907-G-A

74835666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115133971-C-T

74835747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115134028-C-T

http://identifiers.org/hco/17/GRCh38#74835781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115134062-C-A

74835781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115134062-C-T

74835812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115134096-T-C

http://identifiers.org/hco/17/GRCh38#74835871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115134155-C-A

74835871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115134155-C-T

http://identifiers.org/hco/17/GRCh38#74835874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115134158-A-C

74835874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron variant
orthologous variants: 115134158-A-G

74835947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, missense_variant
orthologous variants: 115134216-C-G

74835947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115134216-C-T

http://identifiers.org/hco/17/GRCh38#74835987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115134256-A-C

74835991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115134260-G-A

74835991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115134260-G-C

74835991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115134260-G-T

http://identifiers.org/hco/17/GRCh38#74836045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115134314-C-A

74836045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115134314-C-T

74836110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, missense_variant
orthologous variants: 115134379-G-A

74836132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115134401-G-A

74836249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115134518-C-G

74836249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115134518-C-T

74836424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, missense_variant
orthologous variants: 115134693-C-G

74836424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115134693-C-T

74836483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115134752-G-A

74836501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, stop_gained
orthologous variants: 115134770-C-G

74836501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115134770-C-T

74836564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115134833-G-A

74836564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115134833-G-C

74836567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115134836-C-T

74836742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115135006-T-G

http://identifiers.org/hco/17/GRCh38#74836772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115135037-C-A

74836772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115135037-C-T

http://identifiers.org/hco/17/GRCh38#74836780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115135045-C-A

74836780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115135045-C-T

http://identifiers.org/hco/17/GRCh38#74836878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115135126-C-A

74836878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115135126-C-G

74836878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115135126-C-T

74836952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115135147-C-T

http://identifiers.org/hco/17/GRCh38#74836972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115135166-C-A

74837035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115135217-A-G

74837035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115135217-A-T

http://identifiers.org/hco/17/GRCh38#74837089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115135256-C-A

74837102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115135269-G-A

http://identifiers.org/hco/17/GRCh38#74837183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115135343-C-A

74837228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115135388-G-A

74837228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115135388-G-T

74837297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115135464-A-T

74837417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115135551-C-T

74837432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115135568-G-A

74837432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115135568-G-T

74837482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115135616-G-A

74837504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115135634-G-A

74837504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115135634-G-T

74837532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115135688-G-A

74837532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115135688-G-T

74837585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 115135739-G-A

74837585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 115135739-G-T

74837597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115135762-G-A

http://identifiers.org/hco/17/GRCh38#74837670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115135848-C-A

74837670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115135848-C-T

74837726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115135904-A-G

74837749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115135927-A-G

http://identifiers.org/hco/17/GRCh38#74837756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115135934-C-A

74837756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115135934-C-T

74837757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115135935-A-G

http://identifiers.org/hco/17/GRCh38#74837760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115135938-C-A

74837760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115135938-C-T

74837784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115135962-A-T

74837838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115136010-A-G

74837846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115136018-G-T

http://identifiers.org/hco/17/GRCh38#74837896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115136063-A-C

74837906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115136073-G-A

74837906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115136073-G-T

74837942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136093-G-A

74837942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136093-G-T

http://identifiers.org/hco/17/GRCh38#74838026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115136212-C-A

74838039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136225-G-A

74838039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136225-G-C

74838253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136400-G-A

74838293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136441-C-T

74838366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136530-T-A

74838513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136711-G-A

74838513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136711-G-T

http://identifiers.org/hco/17/GRCh38#74838516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115136714-C-A

74838517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136715-A-G

http://identifiers.org/hco/17/GRCh38#74838578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115136769-C-A

74838578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136769-C-T

74838650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136860-A-G

74838662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136872-C-G

74838662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136872-C-T

74838740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115136951-A-G

74838873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115137099-T-C

74838873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115137099-T-G

74838896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 115137116-C-T

74838897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 115137117-G-A

74838897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 115137117-G-T

74839023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 115137225-T-C

74839113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: 115137295-T-C

74839113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: 115137295-T-G

http://identifiers.org/hco/17/GRCh38#74839361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115137487-C-A

74839361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: 115137487-C-T

http://identifiers.org/hco/17/GRCh38#74839364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115137490-C-A

74839364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: 115137490-C-G

74839364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: 115137490-C-T

74839401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: 115137527-G-A

74839401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: 115137527-G-C

74839401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: 115137527-G-T

74839417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: 115137544-T-C

74839452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: 115137574-T-G

http://identifiers.org/hco/17/GRCh38#74839509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115137648-A-C

74839509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: 115137648-A-G

74839517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: 115137656-G-T

74839530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25984
most severe consequence: 3 prime UTR variant
orthologous variants: 115137665-A-G