63851966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90641954-C-T

63851969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90641957-C-T

63852452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90642199-G-A

63852461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90642208-G-T

63852473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90642219-C-T

63852710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90642460-C-T

63852857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90642584-T-C

http://identifiers.org/hco/13/GRCh38#63852940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90642670-C-A

63852940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90642670-C-T

63853064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90642790-T-C

63853317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90643260-T-G

63853720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90643689-C-T

63853737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90643706-T-C

63853737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90643706-T-G

63853806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90643770-G-T

63854260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90644256-G-A

http://identifiers.org/hco/13/GRCh38#63854466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90644465-C-A

http://identifiers.org/hco/13/GRCh38#63854636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90644622-C-A

63855013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90644992-A-T

http://identifiers.org/hco/13/GRCh38#63857426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90646675-A-C

63857473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90646722-C-G

63858171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90646932-A-T

63858277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90647039-A-T

63858333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90647094-T-C

63858558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90647273-C-T

63858660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90647394-G-A

63858671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90647405-T-C

63858725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90647456-T-C

63858745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90647476-T-C

63858845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90647556-C-T

http://identifiers.org/hco/13/GRCh38#63858916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90647623-C-A

63858918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90647625-C-T

63867670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90649779-G-A

63867770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90649866-T-G

63867816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90649908-T-C

63868093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90650160-A-T

63868967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90650999-T-C

63869430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90651340-G-A

63869443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90651353-T-G

63869551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90651897-T-C

63869666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90652014-T-C

63899834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90684758-T-C

http://identifiers.org/hco/13/GRCh38#63899894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90684830-C-A

63899894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90684830-C-G

63899945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90684881-A-G

63900034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90684965-G-T

63900042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90684973-C-T

63900116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90685044-C-T

63900146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90685074-C-T

http://identifiers.org/hco/13/GRCh38#63900149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90685077-C-A

63900191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90685135-A-G

63900242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90685186-G-A

http://identifiers.org/hco/13/GRCh38#63900311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90685263-C-A

63900435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90685386-C-T

63900485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90685437-A-G

63900499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90685450-T-G

63900801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90685767-T-G

63900810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90685776-C-T

63900853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90685819-C-T

63900943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90685910-A-G

63900956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90685923-T-C

63900993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90685960-G-C

http://identifiers.org/hco/13/GRCh38#63901031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90685998-A-C

63901177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90686130-G-T

63901323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90686262-G-C

63901396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90686317-A-G

63901422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90686332-A-G

63901490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90686391-T-C

63901497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90686399-G-A

http://identifiers.org/hco/13/GRCh38#63901525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90686428-C-A

63901528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90686431-A-G

http://identifiers.org/hco/13/GRCh38#63901547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90686452-C-A

63901547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90686452-C-G

63901566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90686471-T-A

63901566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90686471-T-G

63901585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90686490-A-T

http://identifiers.org/hco/13/GRCh38#63901591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90686496-A-C

63901592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90686497-T-A

http://identifiers.org/hco/13/GRCh38#63901619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90686525-C-A

63901619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90686525-C-G

63901675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90686580-C-T

63905311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90693435-T-C

63905332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90693443-A-G

63905378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90693492-G-A

63905509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90693638-A-G

63905510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90693639-T-C

63905637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90693758-G-T

63905639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90693760-T-G

http://identifiers.org/hco/13/GRCh38#63905687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90693808-A-C

63905724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90693845-C-T

http://identifiers.org/hco/13/GRCh38#63905883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90694004-C-A

63905904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90694025-G-C

63905993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90694116-A-G

63911594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90697998-A-G

63911744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90698130-A-G

http://identifiers.org/hco/13/GRCh38#63911806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90698190-A-C

63912158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90698540-C-T

63912217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90698590-G-C

63912217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90698590-G-T

63912527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90698887-G-A

63912569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90698936-G-A

63912608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90698977-T-C

63912616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90698985-G-A

63912762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90702754-A-G

63913160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90703109-C-T

63913325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90703273-C-T

63913477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90703418-T-G

63913496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90703436-G-A

63913523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90703462-C-T

63940996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90708606-A-T

http://identifiers.org/hco/13/GRCh38#63943503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90713081-C-A

63943637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90714123-G-T

63943760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90714228-A-T

63943828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90714320-A-G

63943918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90714394-T-C

63944108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90714576-A-G

63944299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90714749-G-C

63944451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90714902-T-C

63944819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90715839-T-C

63944855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90715899-C-T

63945138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90716189-T-C

63945258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90716309-C-G

63945546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90716587-A-T

63946085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90717090-T-C

63947946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90718396-A-T

63947960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90718431-G-A

63948375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90718667-G-A

63948486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90718787-T-C

63948607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90718898-T-C

63949166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90719417-T-C

63957229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90724007-A-G

http://identifiers.org/hco/13/GRCh38#63957274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90724052-A-C

63957458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90724264-C-T

63957699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90724534-C-T

63957702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90724537-A-T

63957770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90724598-A-T

63958142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90724867-A-G

63958303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90725028-T-G

http://identifiers.org/hco/13/GRCh38#63958410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90725250-A-C

63958410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90725250-A-G

63958541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90725376-G-A

63959072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90725898-T-C

63959072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90725898-T-G

63960354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90726163-G-T

63961520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90729141-C-G

63961664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90729280-G-T

http://identifiers.org/hco/13/GRCh38#63961681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90729297-C-A

http://identifiers.org/hco/13/GRCh38#63961692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90729306-A-C

63961781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90729390-A-G

http://identifiers.org/hco/13/GRCh38#63961800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90729408-A-C

63961800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90729408-A-G

63961990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90729587-C-G

63962086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90729709-G-T

63962118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90729741-T-A

63962122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90729745-C-G

63962143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90729763-G-T

63962223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90729811-T-C

63962264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90729851-G-A

63962664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90730185-T-C

63962694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90730228-T-C

63962812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90730415-T-C

63962888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90730598-T-C

http://identifiers.org/hco/13/GRCh38#63962941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90730648-C-A

63962977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90730673-C-T

63963078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90730769-C-G

63963351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90731042-G-C

63963870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90731148-A-G

63966608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

63967065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

63967225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90738220-C-G

63967789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90738802-G-C

63972014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90741213-G-C

63972014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90741213-G-T

63972053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90741255-T-C

63972714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90741876-T-C

63973223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90742087-G-A

63973244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90742108-G-T

http://identifiers.org/hco/13/GRCh38#63973358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90742205-C-A

63974196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748142-A-G

63974809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748472-T-C

63974832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748501-A-T

63974881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748550-C-G

63975017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748677-A-G

63975032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748692-C-G

63975076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748734-C-T

63975095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748753-G-A

63975232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748885-G-A

63975321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748972-T-C

63978023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756803-A-G

63978219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756979-C-T

63978346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90757099-T-C

http://identifiers.org/hco/13/GRCh38#63978617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90757358-C-A

63978746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90757486-T-C

http://identifiers.org/hco/13/GRCh38#63979122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90760328-C-A

63979269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760471-T-A

63979269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760471-T-C

63979269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760471-T-G

63979284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760486-T-G

63979300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760502-C-T

63979314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760516-C-T

63979426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760599-G-T

63979586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760734-T-C

http://identifiers.org/hco/13/GRCh38#63979671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90760823-A-C

63979727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760883-A-T

63979761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760913-T-C

63979837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760987-A-G

63980107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761229-T-C

63980115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761237-G-A

63980258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761368-G-A

63980258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761368-G-C

63980258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761368-G-T

63980593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761719-T-A

63980667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761792-A-G

63981272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90762762-G-T

63981328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90762809-T-G

63981374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90762857-G-A

63981403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90762887-T-C

63981521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90763004-A-G

63981531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90763014-C-T

63981715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90763182-A-G

63982143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90763541-G-A

63982197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90763591-C-T

63982348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90763815-G-A

63982524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90764012-C-T

63982603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90764092-T-C

63982656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90764147-T-C

http://identifiers.org/hco/13/GRCh38#63988068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90765672-A-C

63988744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90766325-T-C

63988744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90766325-T-G

63988788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90766360-A-T

63989231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90766729-A-G

63989302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90766796-G-C

63989306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90766800-C-T

63989387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90766901-A-G

63989637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90767128-T-C

63990178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: non coding transcript exon variant
orthologous variants: 90767331-G-C

http://identifiers.org/hco/13/GRCh38#63990198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90767356-C-A

63990664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90767829-C-G

63990664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90767829-C-T

http://identifiers.org/hco/13/GRCh38#63990793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90767954-C-A

63990808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90767969-T-C

63991094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90768220-A-G

http://identifiers.org/hco/13/GRCh38#63991169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90768293-C-A

63991250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90768388-T-G

63991252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90768390-C-T

63991465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90768572-A-T

63991469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90768576-C-T

63991489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90768595-C-T

63995764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90769799-A-G

63995935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90769937-G-C

63996098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90770071-G-C

63996290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90770251-T-G

63996361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90770309-A-G

64005863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

64010487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90794931-A-T

http://identifiers.org/hco/13/GRCh38#64010518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90794958-A-C

64010567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90795004-T-A

64010567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90795004-T-C

64010568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90795005-A-T

64010598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90795034-T-A

64010790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90795238-A-G

64010836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90795284-A-G

64010840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90795287-A-G

64010998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90795428-G-T

64011024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90795457-A-G

http://identifiers.org/hco/13/GRCh38#64011032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90795465-A-C

64011074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90795503-T-C

64011152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90795579-C-T

64011210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90795639-T-C

64011224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90795670-A-G

64014609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90797710-A-G

http://identifiers.org/hco/13/GRCh38#64014714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90797808-C-A

64014726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90797818-C-G

http://identifiers.org/hco/13/GRCh38#64014730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90797822-C-A

http://identifiers.org/hco/13/GRCh38#64014783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90797878-C-A

64014783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90797878-C-T

64014810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90797905-G-A

64014977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90798063-T-C

64015347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90798383-C-G

64015370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90798408-G-A

64015370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90798408-G-T

64015396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90798436-T-C

64015414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90798454-A-G

64015414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90798454-A-T

64015446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90798470-C-G

http://identifiers.org/hco/13/GRCh38#64015470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90798488-A-C

64015639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90798647-G-A

64015639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90798647-G-C

64016294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90798772-A-T

64016625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90799106-C-T

64016694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90799175-C-T

64016728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90799209-C-T

64016820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90799303-T-C

64016891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90799374-C-G

64017124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90799608-A-T

64017132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90799614-G-A

http://identifiers.org/hco/13/GRCh38#64017235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90799713-A-C

64017235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90799713-A-G

64017487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90801966-T-A

64017496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90801975-G-C

http://identifiers.org/hco/13/GRCh38#64017908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90802386-C-A

64017908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90802386-C-T

64017941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90802421-A-G

64017972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90802452-C-T

64018133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90802588-A-G

64018144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90802599-T-A

64018242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90802756-A-G

64018242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90802756-A-T

64018261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90802775-C-T

64018317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90802834-T-A

64018317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90802834-T-G

64018378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90802879-A-G

http://identifiers.org/hco/13/GRCh38#64018526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90803104-A-C

64018563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90803145-A-G

64018598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90803184-A-G

64018691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90803273-G-C

64018721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90803299-C-G

64018821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90803404-C-T

64018938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90803513-G-A

64018938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90803513-G-C

64023412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90805476-T-C

http://identifiers.org/hco/13/GRCh38#64023504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90805570-C-A

64023701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90805757-G-A

64023725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90805782-G-A

64023725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90805782-G-T

64023762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90805823-T-G

64023940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90805988-G-C

64023940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90805988-G-T

http://identifiers.org/hco/13/GRCh38#64023963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90806011-A-C

64023963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90806011-A-G

64024030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90806081-C-T

64024212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90806249-T-C

64024262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90806293-G-A

64024328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90806367-T-C

64024512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90806549-C-T

64030379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90806843-A-G

64032827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90817119-G-T

64032907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90817200-C-T

64033424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90817712-T-C

64034025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90818223-G-A

64034258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90818451-A-G

64034364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90818535-T-C

64034415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90818587-T-C

64034502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90818672-A-G

64034600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90818743-G-A

64034600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90818743-G-C

64034600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90818743-G-T

http://identifiers.org/hco/13/GRCh38#64034664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90818788-A-C

64034664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90818788-A-G

64034828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90818916-A-G

http://identifiers.org/hco/13/GRCh38#64034909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90818991-C-A

http://identifiers.org/hco/13/GRCh38#64035089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90819154-A-C

64035882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90819951-A-G

64039195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90820770-T-C

64039306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90820864-T-C

64039306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90820864-T-G

64039307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90820865-C-G

64039346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90820890-G-A

64039346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90820890-G-T

64039495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90821068-C-T

64041756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90827843-T-A

http://identifiers.org/hco/13/GRCh38#64041765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90827852-A-C

64041765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90827852-A-G

64041765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90827852-A-T

http://identifiers.org/hco/13/GRCh38#64041889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#90827900-C-A

64044938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90834584-G-A

64045029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90834668-C-G

64045196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90834820-G-A

64045196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90834820-G-T

64045391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90835030-T-C

64045476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90835117-T-C

64045638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90835283-A-G

64045697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90835337-A-G

64045871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90835462-A-G

64045898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90835485-C-T

64046013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90835589-T-C

64048682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90842775-T-C

64048709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90842796-T-C

64048791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90842878-C-T

64048797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90842884-T-A

64048864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90842950-G-A

64049054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90843135-T-G

64049108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90843188-C-T

64049153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90843233-G-A

64049211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90843275-A-T

64066238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90856502-T-C

64066411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90856663-T-G

64066640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90856894-C-T

64066671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90856925-T-G

64071186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859991-G-C

64071360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860168-A-G

64071370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860178-T-C

64071416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860221-G-A

64071431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860236-G-C

64071432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860237-G-T

64071460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860265-C-T

64071483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860289-A-G

64071496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860302-C-G

64071705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860480-T-A

64071941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860662-T-C

64072180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860868-G-C

64072415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861065-A-G

64072871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90863177-T-G

64073270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90863558-G-T

64073343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90863627-T-C

64073620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90863915-C-G