64044464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107593799-T-C

http://identifiers.org/hco/18/GRCh38#64044547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107593880-A-C

64044547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107593880-A-T

64044596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107593926-G-A

64044745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107594082-G-A

64044871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107594206-A-G

64044919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107594261-A-G

64045113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107594441-C-G

http://identifiers.org/hco/18/GRCh38#64045314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107594617-C-A

64045314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107594617-C-G

http://identifiers.org/hco/18/GRCh38#64045396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107594687-C-A

64045639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107594915-G-C

64045672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107594954-C-G

64045717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107594994-G-A

64046807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107595736-T-G

64047254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107596172-T-G

64047319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107596236-G-C

http://identifiers.org/hco/18/GRCh38#64047483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107596386-C-A

64047528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107596428-T-G

64053647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107600959-G-A

64053898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107601217-G-A

64054018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107601314-A-G

64054459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107604575-A-G

http://identifiers.org/hco/18/GRCh38#64054471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107604587-C-A

64054471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107604587-C-T

64054480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107604597-G-C

64054527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107604640-C-T

64054611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107604719-T-C

64054678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107604783-C-T

64054926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107605031-C-G

http://identifiers.org/hco/18/GRCh38#64055188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107605289-C-A

64055198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107605297-G-A

64055699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107605802-T-C

http://identifiers.org/hco/18/GRCh38#64055785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107605865-C-A

64055826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107605903-G-T

64057046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107606263-G-C

64057126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107606325-G-A

64057286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107606481-A-G

64057340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107606519-T-A

64057410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107606577-C-T

64057605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107607036-C-T

64058100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107607221-C-G

64061450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107608814-A-G

64061810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107609148-C-G

64061869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107609209-A-G

64061930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107609260-T-G

http://identifiers.org/hco/18/GRCh38#64061943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107609276-A-C

64061943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107609276-A-G

64063851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107609625-G-A

64064006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107609793-T-C

64064083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107609869-G-A

64064335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107610106-A-G

64064380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107610151-T-C

http://identifiers.org/hco/18/GRCh38#64064457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107610227-A-C

64065004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107610715-C-G

http://identifiers.org/hco/18/GRCh38#64065848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107611167-A-C

64071438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107622932-T-C

64071554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107623016-T-G

64071578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107623045-T-A

64071659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107623122-C-T

http://identifiers.org/hco/18/GRCh38#64072124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107623562-C-A

64072124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107623562-C-T

64072132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107623569-T-A

64072147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107623584-C-T

http://identifiers.org/hco/18/GRCh38#64072198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107623629-A-C

64072198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107623629-A-G

http://identifiers.org/hco/18/GRCh38#64072199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107623630-C-A

64072199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107623630-C-G

64072199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107623630-C-T

http://identifiers.org/hco/18/GRCh38#64072210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107623641-C-A

64072210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107623641-C-T

http://identifiers.org/hco/18/GRCh38#64072385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107623785-C-A

64072385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107623785-C-T

64072398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107623798-T-C

http://identifiers.org/hco/18/GRCh38#64072428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107623821-C-A

64072428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107623821-C-G

64072428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107623821-C-T

http://identifiers.org/hco/18/GRCh38#64072448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107623841-C-A

64072448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107623841-C-G

64072448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107623841-C-T

64072468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107623861-A-G

64072472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107623865-T-C

64072477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107623870-G-A

64072477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107623870-G-T

64072542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: non coding transcript exon variant
orthologous variants: 107623937-A-G

http://identifiers.org/hco/18/GRCh38#64072545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107623940-A-C

64072545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: non coding transcript exon variant
orthologous variants: 107623940-A-G

64072553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: non coding transcript exon variant
orthologous variants: 107623947-G-T

64072605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: non coding transcript exon variant
orthologous variants: 107623997-A-G

64074030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107624735-T-C

64074172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107624886-G-A

http://identifiers.org/hco/18/GRCh38#64074218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107624932-C-A

64074218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107624932-C-T

64074335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107625047-A-G

64074517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107625231-G-A

64074664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107625369-C-T

64075208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107625635-A-G

64075235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107625662-T-C

64075238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107625665-A-G

64075424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107625837-G-A

64075429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107625842-C-G

64075429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107625842-C-T

64075539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107625949-T-G

64075636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107626049-G-A

64075803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107626203-T-G

64076022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107626432-C-T

64076121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107626532-T-C

64076184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107626595-T-C

64077121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107627066-T-C

64077238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107627169-G-C

64077254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107627185-T-C

64077254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107627185-T-G

64077399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107627336-A-G

64077399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107627336-A-T

64077403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107627340-G-A

64077403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107627340-G-C

64077403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107627340-G-T

64077482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107627413-G-C

64077539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107627468-C-T

64077806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107627730-T-C

http://identifiers.org/hco/18/GRCh38#64080619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107628229-C-A

64080666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107628284-A-G

64080685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107628301-G-C

64080813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107628829-T-A

64080840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107628856-G-A

64080970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107628999-T-C

http://identifiers.org/hco/18/GRCh38#64080994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107629022-C-A

64080994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629022-C-T

64081043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629074-G-C

http://identifiers.org/hco/18/GRCh38#64081060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107629091-C-A

http://identifiers.org/hco/18/GRCh38#64081137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107629161-C-A

64081137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629161-C-T

64081197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629222-A-G

64081290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629311-G-A

64081290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629311-G-T

64081477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629496-A-G

64082603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629927-C-T

64082754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630049-G-A

64082859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107630141-C-T

64082888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107630160-T-C

64083019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630285-T-C

64083020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630286-A-T

http://identifiers.org/hco/18/GRCh38#64083087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107630350-C-A

64083134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630397-T-C

64083334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630618-G-A

64083453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630727-C-T

64083465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630739-A-G

64083485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630755-C-T

64083643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630916-G-A

64083693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630951-T-A

64083693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630951-T-C

64084886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107632950-T-G

64086213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107633572-A-T

64086302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107633663-G-T

64086414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107633775-T-C

64086527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107633875-C-T

64087036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107634357-T-C

64087672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107635418-G-A

64087672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107635418-G-T

64088202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107635551-A-G

64088379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107635709-C-G

64091997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107637132-C-G

64092100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107637227-G-T

64092657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107637499-C-G

64092716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107637572-C-T

64092854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107637687-T-A

64093289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107638122-C-T

http://identifiers.org/hco/18/GRCh38#64094297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107638437-C-A

64094297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107638437-C-T

64094313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107638456-A-T

64094470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107638597-G-A

64094470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107638597-G-C

64095162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107639312-G-A

64095240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107639387-C-T

64095436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107639572-C-T

64096099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107639982-G-A

64096099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107639982-G-T

64096157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107640043-A-G

64096282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107640180-G-T

64096370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107640386-C-G

64096582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107640702-A-G

64096732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107640825-A-G

64097035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107641140-C-T

64097380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107641504-A-G

http://identifiers.org/hco/18/GRCh38#64097551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107641667-C-A

64097693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107641815-A-G

64097693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107641815-A-T

64097761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107641882-A-G

http://identifiers.org/hco/18/GRCh38#64097772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107641896-C-A

64097865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107642000-C-G

64097865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107642000-C-T

http://identifiers.org/hco/18/GRCh38#64097894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#107642025-C-A

64097894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107642025-C-T

http://identifiers.org/hco/18/GRCh38#64097928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107642059-A-C

64097932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107642063-G-A

64098042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107642151-C-T

http://identifiers.org/hco/18/GRCh38#64098118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107642226-C-A

64098153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642261-C-T

64098154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642262-T-C

64098230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642330-C-T

64098237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642337-G-A

64098395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642494-C-T

64098536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642625-G-T

64098597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107642668-T-C

64098737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642834-T-C

http://identifiers.org/hco/18/GRCh38#64098852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107642950-C-A

64098852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642950-C-T

64098918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642983-T-C

64098924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642989-T-C

64098979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107643038-C-G

64099172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107643212-A-G

64099220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107643251-G-A

64099412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107643452-G-A

64099446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107643483-A-G

64099651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107643694-G-A

64099820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107643857-A-G

64099998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107644054-A-G

64100035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107644092-C-G

64100086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107644139-T-G

64100172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107644253-G-T

64100536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107644582-C-G

64100699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107644716-C-T

64100845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107644957-T-C

64100937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107645043-G-A

64100940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107645046-C-G

64100966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107645071-T-C

64101607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107646716-C-G

64101924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107647004-G-C

http://identifiers.org/hco/18/GRCh38#64102013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107647093-C-A

64102149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107647228-A-G

64102325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107647393-A-G

64102326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107647394-G-A

64102381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107647433-A-G

64103657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107648569-C-T

64103681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107648595-T-C

64103687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107648601-C-T

64103827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107648776-T-C

64103831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107648780-G-C

64103831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107648780-G-T

64103854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107648803-C-T

64104000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107648941-G-A

64104000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107648941-G-T

64104073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107649017-T-G

64104129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107649079-T-A

http://identifiers.org/hco/18/GRCh38#64104310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107649251-C-A

64104310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107649251-C-T

64104474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107649403-C-G

64104474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107649403-C-T

http://identifiers.org/hco/18/GRCh38#64104506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107649435-C-A

64104694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107649627-G-C

64104819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107649687-G-A

64104924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107649792-G-A

http://identifiers.org/hco/18/GRCh38#64104967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107649836-C-A

64105065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107649916-C-G

http://identifiers.org/hco/18/GRCh38#64105471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107650364-C-A

64105491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107650384-A-G

http://identifiers.org/hco/18/GRCh38#64105718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107650601-C-A

64106157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651029-C-T

64106369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651244-C-G

64106438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651310-C-T

64106474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651346-G-A

64106487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651361-C-G

64106733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651585-A-G

64106734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651586-G-A

64106783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651617-G-C

64106999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651832-G-A

64107011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651840-T-C

64107069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651890-T-C

64107076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651897-A-G

64107177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651985-G-A

64107622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107652391-T-C

64107793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107652540-G-C

64107824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107652572-C-G

64107911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107652657-G-A

64107911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107652657-G-T

http://identifiers.org/hco/18/GRCh38#64107953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107652675-A-C

64108177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107652895-C-T

64108182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107652900-T-G

http://identifiers.org/hco/18/GRCh38#64108259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107653001-A-C

64108288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107653030-G-A

64108593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107653311-G-A

http://identifiers.org/hco/18/GRCh38#64108738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107653438-C-A

64108764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107653465-A-G

64108915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107653558-G-A

64109107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107653750-A-G

http://identifiers.org/hco/18/GRCh38#64109219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107653827-A-C

http://identifiers.org/hco/18/GRCh38#64110451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107654301-C-A

64110456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107654303-T-G

64110462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107654309-G-A

64110509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107654358-G-A

http://identifiers.org/hco/18/GRCh38#64110602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107654422-C-A

64110649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107654468-G-A

64110666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107654479-T-C

64110746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107654552-C-T

64110957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107654768-G-C

64111097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107654907-C-T

64111155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107654963-A-G

64111271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107655072-C-T

http://identifiers.org/hco/18/GRCh38#64111276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107655077-A-C

64111368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107655164-C-T

64111385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107655181-C-T

64111386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107655182-G-A

64111410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107655206-A-G

64111724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107656020-T-C

64112164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656464-C-T

64112169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656469-T-C

64112179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656479-G-A

64112194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656494-C-T

64112239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656539-T-C

64112239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656539-T-G

64112274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656574-A-G

64112289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656589-C-T

64112290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656590-G-A

http://identifiers.org/hco/18/GRCh38#64116332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107660251-C-A

64116894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107660638-G-A

64116894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107660638-G-T

64117106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107660836-A-G

http://identifiers.org/hco/18/GRCh38#64117512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107661251-A-C

64117642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107661397-G-A

64117713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662036-C-T

64117783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662102-G-A

64117869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662184-A-G

64117885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662200-A-T

64117887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662202-G-T

64118387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662676-G-A

64118431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662723-T-A

64118533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662815-A-G

http://identifiers.org/hco/18/GRCh38#64118761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107663986-C-A

64119105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107664569-G-A

64119441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107664943-T-C

64119450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107664952-A-G

http://identifiers.org/hco/18/GRCh38#64120179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107666294-C-A

64120209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107666323-C-T

64120719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107667063-C-T

64121004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107667347-T-A

64121109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107667449-C-T

64124424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107669891-C-T

64124799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107670251-T-A

64124965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107670407-G-C

64125061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107670504-G-A

64126786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107674694-G-A

64126836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107674738-A-T

64126953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107674839-T-A

64127289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107675146-T-G

64127382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107675238-C-T

64127384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 107675240-G-A

64127384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 107675240-G-T

64127417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107675271-A-G

64127554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107675412-G-A

64127554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107675412-G-T

64127706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107675572-G-A

64127773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107675625-T-C

64128037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107676407-T-C

64128225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107676590-T-C

64128495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107676863-C-T

64128674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107677040-G-A

http://identifiers.org/hco/18/GRCh38#64128781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107677146-A-C

64128781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107677146-A-G

64129219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107677550-C-G

64129243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107677574-C-T

http://identifiers.org/hco/18/GRCh38#64129245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107677576-C-A

64129500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107677808-A-G

64129730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107678032-T-C

64129730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107678032-T-G

64129752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107678071-T-C

64130326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107678699-A-T

64130330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107678703-C-T

64130369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107687535-G-A

64130369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107687535-G-C

64130499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107687644-C-T

64130553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107687694-C-G

64130572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107687711-G-A

64130572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107687711-G-T

64130939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107688029-C-G

64131002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107688092-T-C

64131233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107688314-C-T

64131362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107688443-C-T

64131545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107688626-T-C

64132184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107689264-A-G

http://identifiers.org/hco/18/GRCh38#64132549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107689586-C-A

64132549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689586-C-T

64132623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689661-G-A

64132670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689706-A-G

64132670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689706-A-T

64132781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689846-G-A

64132898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689945-C-T

64132936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689983-G-A

64132936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689983-G-C

64132936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689983-G-T

64133155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107690178-G-A

64133899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107692539-G-A

64133901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107692541-C-T

64133916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107692556-C-T

64134148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107693476-T-C

64134451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107693776-T-G

64134477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107693802-C-T

64134593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107693911-G-A

64134609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107693927-G-A

64134666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107693987-C-G

64137215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107694314-A-G

http://identifiers.org/hco/18/GRCh38#64137322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107694420-C-A

64137570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107694568-G-T

http://identifiers.org/hco/18/GRCh38#64138515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107695511-C-A

64138515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107695511-C-G

http://identifiers.org/hco/18/GRCh38#64138631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107695624-A-C

64138840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107695882-G-T

64139040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107696078-G-T

http://identifiers.org/hco/18/GRCh38#64139331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107696353-C-A

64139331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107696353-C-T

64139593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107696594-G-A

http://identifiers.org/hco/18/GRCh38#64141801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107701882-C-A

64142105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107702174-G-A

64142105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107702174-G-T

64142398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107702563-G-C

http://identifiers.org/hco/18/GRCh38#64142612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107702776-C-A

64143109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107703861-G-A

64143243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107703964-C-T

64145784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107705183-G-A

http://identifiers.org/hco/18/GRCh38#64145871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107705261-A-C

64145909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107705304-C-T

64145922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107705317-A-G

64145977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107705372-T-C

64146015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107705408-G-A

64146017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107705410-G-T

64146060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107705461-T-C

64146174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107706637-T-C

64146572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107707025-T-A

64146572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107707025-T-C

http://identifiers.org/hco/18/GRCh38#64146610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107707054-C-A

64146702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107707128-T-C

64146873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107707344-C-G

64147045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107707523-T-C

64147359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107707779-G-T

64147411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107707829-T-C

64147685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107708017-C-T

64147815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107708164-G-A

64147880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107708265-G-A

64148171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107709210-T-C

http://identifiers.org/hco/18/GRCh38#64148228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107709243-C-A

64148414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107709405-T-A

64148655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107709601-T-C

64148681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107709624-T-C

64148744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107709664-A-T

64148779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107709699-T-C

64148782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107709702-A-G

64148806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107709716-G-T

64148860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107709775-G-A

64148860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107709775-G-T

http://identifiers.org/hco/18/GRCh38#64148964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107709850-C-A

64148967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107709853-G-T

http://identifiers.org/hco/18/GRCh38#64148969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107709857-C-A

http://identifiers.org/hco/18/GRCh38#64149028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107709897-C-A

64149044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107709913-G-A

64149044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107709913-G-C

64149044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107709913-G-T

http://identifiers.org/hco/18/GRCh38#64149151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107710026-C-A

64149151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107710026-C-T

64149181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107710056-A-G

64149325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107710189-G-T

64149489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107710343-C-T

64149527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107710376-A-G

http://identifiers.org/hco/18/GRCh38#64149702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107710537-C-A

64149782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107710613-C-T

64150012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107710832-C-G

64150012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107710832-C-T

http://identifiers.org/hco/18/GRCh38#64150320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107711139-C-A

64150390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107711202-C-T

64150458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107711298-T-A

64152532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107714804-T-A

64152554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107714826-T-C

64156134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107734266-G-A

64156134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107734266-G-C

64156177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107734308-G-A

64156187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107734318-G-T

64156222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 107734337-A-G

64156305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107734442-A-G

64156305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107734442-A-T

64156336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107734473-A-G

64156364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107734501-T-C

http://identifiers.org/hco/18/GRCh38#64156509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107734624-A-C

64156555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107734668-T-C

64156719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107734808-G-A

64156719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107734808-G-C

64156824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107734899-T-G

64156941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107734985-G-A

http://identifiers.org/hco/18/GRCh38#64156996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107735043-A-C

64157285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107736961-A-G

http://identifiers.org/hco/18/GRCh38#64157329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107737005-A-C

64157529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107737252-T-C

64157578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107737301-G-C

64157578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107737301-G-T

http://identifiers.org/hco/18/GRCh38#64157748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107737465-C-A

64157872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107737586-G-A

64158412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107741927-G-T

64158560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107742069-C-T

64158589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107742098-G-A

64158718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107742224-T-C

http://identifiers.org/hco/18/GRCh38#64158816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107742313-C-A

64158816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107742313-C-T

http://identifiers.org/hco/18/GRCh38#64159029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107742510-A-C

64159106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107742583-G-T

64159140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107742620-T-C

http://identifiers.org/hco/18/GRCh38#64159237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107742729-C-A

64159949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107744638-G-A

64160104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107744776-T-G

64160294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107744943-G-A

http://identifiers.org/hco/18/GRCh38#64160617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107745206-A-C

64160617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107745206-A-G

64160618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107745207-T-G

64160864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107745419-G-A

64161097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107745637-G-A

64161248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107745791-C-T

64161352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107745883-T-C

64161476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107745992-T-C

64161623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107746100-G-A

64161719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107746201-A-G

64161885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107746356-T-C

64162041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107746513-C-T

64162575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107746994-C-G

64163758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107750222-A-G

64163758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107750222-A-T

64163845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107750303-T-C

64164238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107757882-G-T

64164329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107757987-G-A

64164337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107757995-T-A

64164695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107764230-C-T

64164766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107764299-C-T

64164812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107764345-G-T

64164820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107764353-T-C

64164866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107764399-C-T

64164986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107764506-C-T

64165772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107765444-G-A

64166157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107765843-G-A

64166276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107765956-G-T

64166311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107765991-G-A

64166725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107766357-A-G

64166823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107766448-G-A

64167034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107766647-G-A

64167830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107768419-A-G

64168019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107768622-C-G

64168019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107768622-C-T

64168234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107768797-G-A

64168234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107768797-G-T

64168520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107769015-T-C

64168567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107769059-A-G

64168630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107769123-A-G

64168657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107769150-T-G

64168939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107769417-T-A

64168952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107769430-G-A

64169446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107769968-T-C

64169705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107770472-T-C

64169745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107770515-C-T

64169927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107770707-G-C

64170164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107770952-A-G

64170198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107770985-T-A

64170198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107770985-T-C

64170330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107771105-C-T

64170378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107771154-C-T

http://identifiers.org/hco/18/GRCh38#64170492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107771245-A-C

64174221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107772269-C-T

http://identifiers.org/hco/18/GRCh38#64174457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107772356-C-A

64174473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107772372-G-A

64174503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107772400-G-A

64174514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107772411-C-T

64174643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107772532-C-T

64176001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107775013-C-G

64176001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107775013-C-T

64179612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107775497-C-T

64179884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107775758-C-T

64180184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107776261-G-A

64180191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107776268-G-A

64180584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107776709-A-T

64180632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107776755-A-G

64180643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107776766-T-C

64180653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107776776-A-G

64180824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107776939-G-A

http://identifiers.org/hco/18/GRCh38#64181123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107777222-A-C

64181326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107777462-T-C

64181661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107777687-T-C

64182318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107778295-C-T

64182509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107778487-G-A

64182574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107778552-G-T

http://identifiers.org/hco/18/GRCh38#64182919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107778857-A-C

64182919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107778857-A-T

64183018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107778940-C-G

64183194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107779085-A-G

http://identifiers.org/hco/18/GRCh38#64183618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107781244-A-C

64183618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107781244-A-G

64183695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107781315-C-T

64183702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107781322-C-T

64183826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107781443-A-G

http://identifiers.org/hco/18/GRCh38#64183835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107781451-C-A

64183885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107781506-G-C

64183977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107781595-T-C

64184089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107781708-G-A

64184107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107781726-T-C

64184154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107781763-C-G

64184285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107781865-A-G

64184376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107781911-A-G

64184825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107782298-C-T

http://identifiers.org/hco/18/GRCh38#64184955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107782430-A-C

64185166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107786591-T-A

64185166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107786591-T-C

64185170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107786595-C-T

64185854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107786889-G-T

64186141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107787218-G-C

64186250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107787319-C-T

64186302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107787352-G-C

64186371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107787419-T-C

64186377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107787423-G-A

64186721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107787607-G-A

64186749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107787636-G-A

64187137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107788008-C-G

64187387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107788257-A-G

64187569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107788438-T-C

64188121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107788737-C-T

64188181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107788796-T-C

64188309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107788911-G-C

http://identifiers.org/hco/18/GRCh38#64188402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107788989-C-A

64188481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107789068-A-G

http://identifiers.org/hco/18/GRCh38#64188655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107789246-C-A

64188726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107789313-G-A

64188883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107789465-C-T

http://identifiers.org/hco/18/GRCh38#64189453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107790083-C-A

64189453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107790083-C-T

64189599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107790249-A-G

64189738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107790369-C-T

64189752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107790383-T-G

64189938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107790546-G-A

64190692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107791589-C-T

64190777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107791691-A-G

64190787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107791701-A-T

64190856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107791768-T-C

64190927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107791840-G-A

64190991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107791902-G-A

64190991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107791902-G-T

64191266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107792163-G-T

64193481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107793614-G-A

64193529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107793662-G-A

64193552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107793677-C-G

64193959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107793774-C-T

64193978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107793793-T-C

64194057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107793884-T-C

64194095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107793920-G-A

64194095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107793920-G-C

64194397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107794210-C-T

http://identifiers.org/hco/18/GRCh38#64194510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107794325-C-A

64194523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107794344-A-G

64194678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107794477-C-T

http://identifiers.org/hco/18/GRCh38#64194783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107794558-A-C

64194813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107794587-T-C

64195086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107794803-G-C

64196572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107799101-C-T

64196573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107799102-A-G

64196674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107799190-T-C

64196704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107799215-T-A

64196706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107799217-C-T

64196710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107799221-A-G

64196780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107799283-T-C

64196870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107799365-T-C

64196896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107799391-G-T

64196976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107799475-T-A

64197308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107799784-T-C

64198207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107800021-C-T

64198297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107800105-A-G

64199518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107802861-A-T

64199598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107802928-G-A

64199750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803066-T-A

64199940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803228-G-T

64200298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803572-C-T

http://identifiers.org/hco/18/GRCh38#64200458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107803712-C-A

64200484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803737-G-A

64200484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803737-G-T

64200663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803834-G-C

64200663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803834-G-T

64200695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803851-G-A

64200767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803896-G-A

64200807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107803937-C-G

64200979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107804107-C-G

64200979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107804107-C-T

http://identifiers.org/hco/18/GRCh38#64200988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107804116-C-A

64200988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107804116-C-G

64200988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107804116-C-T

64201046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107804162-T-C

64201271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107804469-G-A

64201307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107804501-C-T

64201472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107804648-A-G

64202192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107805297-T-A

64202295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107805400-T-C

64202311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107805416-G-A

64202333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107805436-C-T

64202343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107805447-T-C

64202597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107805707-C-G

64202669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107805772-C-T

64206175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107819954-A-G

64206511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107820252-G-A

64207515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107823128-G-A

64207586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107823175-C-T

64207614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107823660-T-A

64207895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107823955-G-A

64207895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107823955-G-C

64207931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107823991-A-G

64208005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107824075-T-C

http://identifiers.org/hco/18/GRCh38#64208093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107824163-C-A

64209727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107825187-G-C

64209749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107825211-T-C

64210091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107825539-T-C

64210307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107825755-C-G

64210307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107825755-C-T

64210333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107825782-T-C

64210638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107826090-A-G

http://identifiers.org/hco/18/GRCh38#64210761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107826236-C-A

64211089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107826524-G-A

64211089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107826524-G-C

64211301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107826761-C-T

http://identifiers.org/hco/18/GRCh38#64211353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107826814-A-C

64211451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107826913-G-A

64211516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107826979-A-G

http://identifiers.org/hco/18/GRCh38#64211590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107827047-A-C

64211649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107827100-C-T

64211910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107827236-A-G

64211972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107827277-A-G

64212247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107827559-T-C

http://identifiers.org/hco/18/GRCh38#64212436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107827997-A-C

64212459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107828019-T-G

64212618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107828178-G-T

64213017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107828583-G-T

64213123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107828692-A-G

64213135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107828704-C-T

64213182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107828751-T-C

http://identifiers.org/hco/18/GRCh38#64213202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107829355-C-A

http://identifiers.org/hco/18/GRCh38#64213599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107829755-C-A

64213604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107829760-A-G

64213614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107829770-A-G

64213625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107829781-A-G

64213740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107829896-T-G

64213746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107829902-G-A

64213801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107829953-T-C

64213889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107830050-A-G

64213945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107830108-A-G

64213990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107830149-T-C

64214134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107830292-G-A

64214213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107830375-C-T

http://identifiers.org/hco/18/GRCh38#64214309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107830472-C-A

http://identifiers.org/hco/18/GRCh38#64214400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107830569-C-A

64214439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107830590-T-G

64214445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107830596-C-T

64214492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107830627-A-G

http://identifiers.org/hco/18/GRCh38#64214493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107830628-C-A

http://identifiers.org/hco/18/GRCh38#64214516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107830651-C-A

64214544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107830683-G-T

64214577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107830707-A-T

http://identifiers.org/hco/18/GRCh38#64214626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107830727-C-A

64214626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107830727-C-T

64214627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107830728-C-T

64214680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107830748-A-G

64215078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107831151-T-C

http://identifiers.org/hco/18/GRCh38#64215143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107831186-C-A

64215195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107831238-A-G

64215431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107831460-T-C

64215513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107831516-G-A

64215567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107831569-T-C

64216021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107831967-G-C

64216037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107831985-A-G

64216618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107832467-G-A

64216697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107832533-T-C

64216910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107832722-T-G

64216915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107832727-G-T

64216963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107832776-C-T

64217266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107833055-T-C

http://identifiers.org/hco/18/GRCh38#64217335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107833132-C-A

64217335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107833132-C-T

http://identifiers.org/hco/18/GRCh38#64217397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107833177-C-A

64217397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107833177-C-T

64217430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107833210-T-C

64217633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107833413-A-G

64217777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107833536-C-G

64217826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107833584-G-A

64217876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107833622-C-T

64217880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107833626-A-G

64217909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107833656-T-C

64217984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107833725-G-A

64217984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107833725-G-T

64217992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107833733-C-G

64217994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107833735-G-A

64218294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107834931-T-C

64218355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107834987-T-C

64218434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107835073-G-T

64218454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107835093-T-G

http://identifiers.org/hco/18/GRCh38#64218459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107835098-A-C

64218492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107835134-T-G

64218565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107835198-G-A

64218680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107835304-A-G

64218764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107835389-G-A

64218794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107835422-A-G

http://identifiers.org/hco/18/GRCh38#64219047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107835605-C-A

64219047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107835605-C-T

64219086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107835644-G-A

64219086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107835644-G-T

64219128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107835685-C-G

64219272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107835828-T-A

64219610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107836227-G-A

64220016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107836627-G-T

64220372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107838133-T-C

64225209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107838960-G-C

64225278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107839039-C-T

64225303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107839063-G-T

64225475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107839285-G-T

64225499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107839309-G-A

64225691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107839463-T-C

64225795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107839547-G-A

64226247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107839953-C-T

64232743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107840354-G-A

64232879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107840457-T-C

64232892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107840470-C-T

64233021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107841423-C-T

64233151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107841571-C-G

64233683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107841803-T-C

64233988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107842046-A-G

64234041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107842099-T-C

64234186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107842247-G-A

http://identifiers.org/hco/18/GRCh38#64234259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107842309-A-C

64234437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107842492-T-A

64234437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107842492-T-C

64234692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107842753-A-G

64234894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107842950-G-A

64235777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107843101-T-C

64235989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107843347-A-T

64236414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107843760-G-T

64236765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107844377-G-A

64236782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107844398-G-A

64238444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107845701-C-G

64238446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107845703-C-G

64238624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107845764-A-G

64238646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107845786-T-C

64239022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107846247-A-G

http://identifiers.org/hco/18/GRCh38#64239070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107846294-C-A

64239070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107846294-C-T

64239234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107846458-T-C

64239291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107846514-C-G

64239349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107846573-C-T

64240019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107847183-A-G

64240580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107854540-G-A

64240580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107854540-G-C

http://identifiers.org/hco/18/GRCh38#64240870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107854826-C-A

64240870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107854826-C-T

64240888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107854844-C-T

64240920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107854874-A-G

64241269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107855188-C-T

64241601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107856430-T-C

64241796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107856562-A-T

64242204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107857053-A-T

http://identifiers.org/hco/18/GRCh38#64242216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107857056-C-A

64242216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107857056-C-T

http://identifiers.org/hco/18/GRCh38#64243718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107858655-C-A

64243728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107858665-A-G

64243786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107858719-A-G

64243946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107858848-C-T

64244413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107859281-T-C

64244541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107859550-T-C

64244802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107861976-G-A

64244998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107862191-G-A

http://identifiers.org/hco/18/GRCh38#64245131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107862325-A-C

64246573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107864289-G-A

http://identifiers.org/hco/18/GRCh38#64246880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107864558-C-A

64246906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107864582-C-T

http://identifiers.org/hco/18/GRCh38#64246977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107864654-C-A

64247242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107864883-T-C

http://identifiers.org/hco/18/GRCh38#64250205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107865105-C-A

64250503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107865361-C-T

64250523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107865375-C-T

http://identifiers.org/hco/18/GRCh38#64251049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107866631-C-A

64251165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107866759-A-G

64251269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107866902-A-G

64251455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107867147-T-C

64251771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107867424-G-C

64251801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107867454-A-G

64251880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107867504-G-T

64251947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107867543-G-C

64251953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107867549-C-G

64251953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107867549-C-T

64252639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107868180-A-G

64252966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107868461-A-G

64252977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107868472-C-T

64253405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107869228-A-T

http://identifiers.org/hco/18/GRCh38#64253656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107869463-A-C

64253665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107869472-G-T

64253712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107869489-A-G

64254460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107870228-G-T

64254652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107870389-G-T

64257017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107872879-T-C

64257018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107872880-A-G

64257740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107873281-G-A

64257838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107873384-G-T

64258005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107873541-G-T

64258133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107873665-A-T

64258155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107873686-G-T

64258655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107877172-A-T

64258685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107877201-C-T

64259035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107877485-T-A

http://identifiers.org/hco/18/GRCh38#64259073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107877523-C-A

64259202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107877645-A-G

64259240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107877684-C-T

64259330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107877778-G-A

http://identifiers.org/hco/18/GRCh38#64260091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107878474-C-A

64260091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107878474-C-T

64260132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107878507-A-G

64260142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107878517-G-T

64260165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107878540-C-T

http://identifiers.org/hco/18/GRCh38#64260166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107878541-C-A

64260166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107878541-C-G