64684892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92917347-C-G

64685010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92917469-G-T

http://identifiers.org/hco/3/GRCh38#64685063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92917520-C-A

64685063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92917520-C-T

64685122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92917577-A-G

64685142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92917597-G-A

64685325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92917779-C-T

64685396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92917848-A-G

64685414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92917867-G-A

64685414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92917867-G-T

64685455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92917914-G-A

64685473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92917932-G-A

64685473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92917932-G-T

64685671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92918135-C-G

64685671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92918135-C-T

64685687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92918152-G-A

64685696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92918161-A-G

64685814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92918263-G-A

64686538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92918998-G-A

64686538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92918998-G-T

64686577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92919037-G-A

64687202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919665-A-G

64687259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919724-G-C

64687301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919765-G-A

64687301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919765-G-T

64687417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919884-A-G

64687501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919966-G-A

64687520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919985-C-G

64687520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919985-C-T

http://identifiers.org/hco/3/GRCh38#64687522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92919987-C-A

64687522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919987-C-G

64687522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92919987-C-T

64687536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92920015-T-C

http://identifiers.org/hco/3/GRCh38#64687614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92920093-C-A

64687614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92920093-C-T

64687980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92920453-G-A

64687980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92920453-G-C

64687980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92920453-G-T

64688004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92920477-G-A

64688004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92920477-G-T

64688179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92920635-G-T

64688381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92920832-T-C

http://identifiers.org/hco/3/GRCh38#64688576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92920996-A-C

64688670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92921094-A-G

64688826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92921252-G-A

64688862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92921287-T-C

http://identifiers.org/hco/3/GRCh38#64688911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92921338-C-A

64688971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92921395-G-T

http://identifiers.org/hco/3/GRCh38#64689169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92921642-C-A

64689192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92921665-G-A

64689233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92921702-A-G

64689376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92921824-G-T

64689864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92922378-C-T

64689920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92922639-T-C

http://identifiers.org/hco/3/GRCh38#64689975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92922693-C-A

64690071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92922825-T-G

64690085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92922839-A-G

64690167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92922920-G-A

http://identifiers.org/hco/3/GRCh38#64690209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92922957-C-A

64690209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92922957-C-T

64690970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92924210-C-G

64691020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92924260-T-C

64691103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92924344-C-T

64691372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92924579-G-A

64691406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92924613-C-T

64691617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92924917-T-C

64691663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92924964-C-T

64691951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92925351-T-A

64692173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92925707-C-T

http://identifiers.org/hco/3/GRCh38#64692231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92925759-C-A

64692231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92925759-C-T

http://identifiers.org/hco/3/GRCh38#64693820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92928379-A-C

64694037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92928573-C-T

64694362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92928927-C-T

64694464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92929013-A-G

64694464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92929013-A-T

64694642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92929179-A-T

64694679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92929216-T-C

64694806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92929345-T-A

64694920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92929459-A-G

64694921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92929460-G-C

64694924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92929463-T-A

http://identifiers.org/hco/3/GRCh38#64694952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92929491-C-A

64694952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92929491-C-T

64695299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92929738-G-C

http://identifiers.org/hco/3/GRCh38#64695316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92929755-C-A

http://identifiers.org/hco/3/GRCh38#64695322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92929761-C-A

64695338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92929771-A-G

64695338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92929771-A-T

64695566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92929992-T-C

64695619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92930029-T-C

64701652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92932594-G-A

64701830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92932759-A-G

64701936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92932850-T-C

64702184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933134-T-G

64702240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933171-G-T

64702244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933175-G-C

64702302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933223-A-G

64702439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933363-A-G

64702511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933428-G-A

64702521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933438-G-A

64702723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933635-G-A

64702724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933636-C-G

64702769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933677-T-C

64702825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92933734-G-T

64703291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92934134-T-C

64703411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92934212-G-A

64703485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92934246-C-T

64703562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92934311-A-G

64703647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92934387-G-A

64705494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92935558-T-C

http://identifiers.org/hco/3/GRCh38#64705666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92935725-A-C

64705686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92935746-A-G

64706158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92936482-G-T

64706159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92936483-G-C

64706348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92936849-T-C

http://identifiers.org/hco/3/GRCh38#64706413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92936900-A-C

http://identifiers.org/hco/3/GRCh38#64706467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92936954-C-A

64706595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92937070-T-C

64706620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92937095-G-A

64706714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92937169-G-T

64706780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92937226-G-A

64706928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92937345-G-A

http://identifiers.org/hco/3/GRCh38#64709091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92937618-C-A

64709091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92937618-C-T

64710851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92938006-G-A

64710851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92938006-G-T

64710889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92938033-C-G

64710889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92938033-C-T

64710960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92938094-G-A

64711476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92938773-T-G

64711477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92938774-T-A

http://identifiers.org/hco/3/GRCh38#64711690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92938951-C-A

64711712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92938973-A-G

http://identifiers.org/hco/3/GRCh38#64711750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92939013-A-C

64711750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92939013-A-G

64711767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92939014-C-G

64711838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92939081-G-A

64711957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92939167-G-A

64712188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92939394-C-T

64712292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92939493-C-G

64712668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92939923-G-T

64712689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92939943-C-T

64712972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92940225-C-G

64713061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92940277-T-C

64713061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92940277-T-G

64713308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92940541-A-G

http://identifiers.org/hco/3/GRCh38#64713320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92940553-C-A

64713346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92940572-G-A

http://identifiers.org/hco/3/GRCh38#64713388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92940603-C-A

64715242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945258-G-A

64715242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945258-G-C

64715335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945351-G-A

64715586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945636-A-G

64715609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945659-T-G

64716019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945718-G-A

64716071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945779-G-C

64716098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945804-T-A

64716098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945804-T-C

64716134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945839-T-A

64716134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945839-T-C

64716137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945842-T-G

64716186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92945897-A-G

64716721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92946418-G-T

64716825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92946518-A-G

64717044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92946749-T-C

64717086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92946798-C-G

64717275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92946984-T-A

64717299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92947046-T-A

64717543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92947421-G-A

64717694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92947580-C-T

64717738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92947623-A-G

64717955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92947811-G-A

64717955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92947811-G-T

64718069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92947923-G-A

64718246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92948094-G-C

64718315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92948164-G-C

64718546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92948393-C-G

64718609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92948466-C-G

64718800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92950234-C-T

64719009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92950433-A-G

64719020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92950444-G-A

64719021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92950445-G-A

64719021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92950445-G-T

64719094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92950515-G-A

64719116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92950537-G-A

64719186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92950606-A-G

64719224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92950644-A-G

64719544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92950942-A-G

64719597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92950997-C-T

http://identifiers.org/hco/3/GRCh38#64719601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92951001-A-C

http://identifiers.org/hco/3/GRCh38#64719654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92951054-C-A

64719656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951056-C-T

64719690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951090-G-A

http://identifiers.org/hco/3/GRCh38#64720198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92951531-C-A

64720226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951559-T-A

http://identifiers.org/hco/3/GRCh38#64720277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92951615-A-C

64720305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951643-C-T

64720329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92951667-T-C

64720592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92952112-C-T

64720628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92952148-A-T

64720638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92952164-A-T

64722055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92955899-T-A

64722474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92956242-A-G

64722488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92956257-G-A

64722505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92956274-A-T

64722580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92956337-T-G

64722810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92956582-G-C

64722948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92956712-T-C

64722966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92956730-G-A

64722973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92956737-C-T

64724116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92957893-G-A

64724160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92957936-A-G

64724250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92958023-C-G

64724379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92958144-A-T

64724483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92958433-A-G

64724538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92958493-T-A

64724573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92958528-T-G

64724709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92958646-T-C

64725140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92959079-G-A

64725245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92959542-A-G

64725435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92959751-G-T

64725708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92960626-C-T

64726529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92961980-T-A

64726529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92961980-T-C

64726623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92962098-A-G

64726664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92962139-C-T

64726930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92962554-G-A

64726965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92962583-C-T

http://identifiers.org/hco/3/GRCh38#64726977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92962595-A-C

64727084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92962878-A-G

64727227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92962987-G-C

64727682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92964233-G-C

64727731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92964293-G-T

64728190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92964598-T-C

64728197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92964605-C-T

64728850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92965212-C-T

http://identifiers.org/hco/3/GRCh38#64728997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92965361-A-C

64736024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92967128-G-A

64737201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92967951-G-A

64737258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968006-T-A

64737375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968100-A-G

64737378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968103-C-T

64737448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968180-T-C

64737519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968251-G-A

64737519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968251-G-T

64738664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968416-A-G

64738709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968439-G-A

64738711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968441-A-G

64738985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968691-G-C

http://identifiers.org/hco/3/GRCh38#64739052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92968760-A-C

64739219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92968875-C-T

64739736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92969670-T-C

64740155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92970092-G-A

64740195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92970132-G-A

64740277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92970213-G-A

64740279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92970215-G-A

64740341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92970260-G-A

64740368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92970287-C-T

64740554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92970473-G-T

http://identifiers.org/hco/3/GRCh38#64740566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92970493-A-C

64740672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92970596-A-G

64740678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92970602-G-A

64741943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92975313-A-G

http://identifiers.org/hco/3/GRCh38#64741998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92975368-A-C

64741998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92975368-A-G

64741998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92975368-A-T

64742000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92975370-A-G

64742118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92975458-G-A

64742118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92975458-G-T

64742841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92975945-C-T

64742895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92975992-T-A

64742928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92976033-T-C

64743053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92976177-T-G

64743253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92976400-T-A

64743534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92976676-T-G

64743629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92976751-C-T

64743785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92976907-A-G

64743883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92977012-T-A

64743947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92977081-G-A

64744177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92977727-A-G

64744178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92977728-T-C

64744292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92977851-G-C

64744467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92977994-A-T

http://identifiers.org/hco/3/GRCh38#64744613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92978103-C-A

64744671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978159-G-A

64744671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978159-G-C

64744758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978242-T-C

http://identifiers.org/hco/3/GRCh38#64744935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92978405-A-C

64745086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978552-C-G

64745086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978552-C-T

64745357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978787-C-T

64745392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978820-T-C

64745454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978882-C-T

64745478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92978905-C-T

64746021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92979522-G-A

64746052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92979557-G-A

http://identifiers.org/hco/3/GRCh38#64746173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92979639-C-A

64746299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92979762-T-C

64747466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92981342-C-G

64747494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92981371-C-T

64747557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92981433-T-A

64747557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92981433-T-G

64747596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92981470-C-T

64747685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92981557-T-G

64747938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92981800-G-A

64747945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92981807-G-T

64747969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92981829-G-A

64748055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92981914-A-G

64748094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92981953-G-C

64748126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92981985-T-C

64748194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92982042-G-T

64748452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92982317-G-A

64749001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92982853-A-G

64755413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92987258-T-G

64755429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92987273-T-G

64755455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92987299-T-A

64755708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92987515-T-C

64756089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92987860-G-A

64756089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92987860-G-C

64756657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92988627-A-G

64757061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92989198-G-C

64757077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92989213-G-A

64758252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92990153-G-T

64758287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92990189-A-G

64758355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92990271-T-C

64758745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92990570-T-G

64761931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92991491-G-T

64762015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92991565-G-C

http://identifiers.org/hco/3/GRCh38#64762208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92991834-A-C

64762229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92991889-C-T

64762240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92991920-G-C

64762395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92992075-C-T

64762461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92992145-C-G

64762461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92992145-C-T

64762822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92992525-T-C

64762965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92992670-C-T

64763106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92992804-T-C

64763140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92992839-G-C

64763839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92993105-C-G

64763839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92993105-C-T

64763954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92993208-C-T

64763957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92993211-A-G

64764159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92993367-C-T

64764237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92993452-A-G

64764310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92993523-T-A

64764310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92993523-T-G

http://identifiers.org/hco/3/GRCh38#64764539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92993763-C-A

64764549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92993861-T-G

64764571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92993984-G-A

64764589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92994000-G-A

64765182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92994504-G-T

http://identifiers.org/hco/3/GRCh38#64765501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92995158-C-A

64765501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92995158-C-T

64765559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92995208-C-T

http://identifiers.org/hco/3/GRCh38#64765596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92995245-C-A

64765596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92995245-C-T

64765653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92995302-T-C

64765723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92995372-C-T

64765767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92995420-G-A

64765816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92995469-T-A

64766033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92995714-A-T

64766267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92995947-G-A

64766430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92996078-C-T

64766912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92996561-A-G

64766918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92996567-G-A

http://identifiers.org/hco/3/GRCh38#64767174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92996798-C-A

64767299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92996922-G-A

64770521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93000588-C-T

64770638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93000711-A-G

64770876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93000908-C-G

64770876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93000908-C-T

64771912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93001232-A-G

64771941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93001261-T-C

64771979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93001300-T-A

64771996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93001317-G-C

64772008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93001329-G-T

64773086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93003035-C-G

64773086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93003035-C-T

64773179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93003126-G-A

64773560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93003514-G-A

64773653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93003608-T-C

64773698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93003656-T-G

64775281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004178-A-G

64775287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004184-T-C

64775385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004271-G-A

64775535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004420-T-A

64775641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004539-C-T

64775648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004546-C-T

http://identifiers.org/hco/3/GRCh38#64775685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93004584-A-C

64775685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004584-A-G

64775867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004860-T-A

64775867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004860-T-C

64775867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004860-T-G

64775908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93004899-C-G

64776008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005011-A-G

64776091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005105-C-T

64776181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005194-G-C

64776277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005285-C-G

http://identifiers.org/hco/3/GRCh38#64783355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93005659-C-A

64783548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005835-T-C

http://identifiers.org/hco/3/GRCh38#64783598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#93005882-A-C

64783598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93005882-A-G

http://identifiers.org/hco/3/GRCh38#64783615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93005898-A-C

64783693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93005973-A-G

64783708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93005988-C-G

64783709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93005989-C-T

64783722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93006003-G-A

64783749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93006021-G-C

64783841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93006115-T-A

64783843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93006117-T-A

64792656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93023778-G-C

http://identifiers.org/hco/3/GRCh38#64793048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93024757-C-A

64793196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93024978-G-A

64793312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93025089-G-A

64793458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93025245-A-G

64793652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93025428-T-C

64793824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93025554-G-C

64797260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036256-C-T

64797313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036307-C-T

64797353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036345-G-T

64797449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036428-T-A

64797503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036459-C-T

http://identifiers.org/hco/3/GRCh38#64797608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93036563-C-A

64797647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036600-C-G

64797698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036651-C-T

64797758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93036703-G-T

64798088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037010-G-C

64798253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037169-G-T

64798293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037222-C-G

64798480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037398-G-A

64798674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037571-G-C

http://identifiers.org/hco/3/GRCh38#64798677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93037574-C-A

64798746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93037637-C-T

64799255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93038469-G-T

64799362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93038583-C-T

64799436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93038655-A-G

http://identifiers.org/hco/3/GRCh38#64799512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93038820-A-C

http://identifiers.org/hco/3/GRCh38#64799520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93038828-C-A

http://identifiers.org/hco/3/GRCh38#64799649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93038959-C-A

http://identifiers.org/hco/3/GRCh38#64799705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93039020-C-A

64799793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93039107-T-A

64799793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93039107-T-C

64799875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93039197-A-G

64799932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93039253-T-C

64800120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93039437-G-T

64800121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93039438-C-T

64800123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93039440-G-T

64800191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93039511-A-G

http://identifiers.org/hco/3/GRCh38#64800243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93039569-C-A

64800314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93039689-T-C

64800359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93039732-G-A

64800359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93039732-G-C

64800359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93039732-G-T

64800471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93039825-T-C

http://identifiers.org/hco/3/GRCh38#64800479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93039833-C-A

64800479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93039833-C-T

http://identifiers.org/hco/3/GRCh38#64800538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93039877-C-A

64801168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93040172-T-C

64801233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93040232-G-A

64801270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93040269-C-T

64801349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93040327-T-C

64801433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93040411-C-T

http://identifiers.org/hco/3/GRCh38#64801575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93040539-C-A

64801709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93040664-C-T

64801807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93040754-A-G

64801807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93040754-A-T

64801978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93040919-G-A

64801978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93040919-G-T

64801989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93040930-G-T

64802012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93040953-G-A

64802146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93041071-G-A

64802146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93041071-G-T

64802160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93041085-A-G

64802287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93041304-G-T

64802299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93041316-G-A

64802299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93041316-G-T

http://identifiers.org/hco/3/GRCh38#64802310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93041327-C-A

64802494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93041760-G-A

64802494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93041760-G-T

http://identifiers.org/hco/3/GRCh38#64802543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93041806-C-A

64802543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93041806-C-T

64802582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93041838-G-T

64802642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93041902-G-A

64803115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042174-G-T

64803124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042188-G-A

64803124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042188-G-T

64803435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042454-C-T

64803979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042545-G-A

64804070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042626-A-G

64804211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042752-T-G

64804428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93042963-A-G

64804781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93043288-C-T

64805040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93043501-C-G

64805040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93043501-C-T

64805153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93043608-G-A

64805217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93043666-T-G

64805692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93044134-G-T

64805996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93044407-C-T

64806017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93044426-A-T

64806052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93044455-T-A

http://identifiers.org/hco/3/GRCh38#64806620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93045073-A-C

64806620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045073-A-G

64807617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045207-C-G

64807617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045207-C-T

64807718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045289-A-T

64807736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045307-A-T

64807800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045353-T-C

64807953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045980-A-G

64807953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93045980-A-T

64808070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046422-G-T

64808187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046529-G-A

64808318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046582-T-C

64808416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046671-C-T

http://identifiers.org/hco/3/GRCh38#64808484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93046730-A-C

64808635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93046855-G-C

64809195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93047409-T-A

64809195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93047409-T-C

64809275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93047461-C-T

64809583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93047904-A-G

64809605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93047927-A-G

http://identifiers.org/hco/3/GRCh38#64809612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93047934-C-A

64809626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93047949-G-A

64809650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93047982-A-G

64809677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93048006-G-T

http://identifiers.org/hco/3/GRCh38#64809683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93048016-C-A

64809699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93048033-A-G

64809737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93048070-A-G

64810447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93049013-T-A

64810697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93049287-G-C

64810783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93049388-G-T

http://identifiers.org/hco/3/GRCh38#64811286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93049559-C-A

http://identifiers.org/hco/3/GRCh38#64811337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93049605-C-A

64811782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93050019-T-A

64811818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93050054-C-G

64811818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93050054-C-T

64811835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93050072-C-T

64812617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93050907-T-G

64813185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93051143-G-A

64813799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93051472-T-C

64813845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93051518-A-G

64814159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93051820-G-A

64814345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93052009-A-G

64814345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93052009-A-T

64814416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93052096-A-T

64814439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93052119-T-G

64815256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93052911-C-T

64815302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93052967-T-A

64815302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93052967-T-C

64815405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053060-G-A

64815779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053359-G-T

64815858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053542-A-T

64816148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053804-G-T

64816256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053915-T-C

64816302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93053963-G-A

64816509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93054168-C-G

64816550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93054210-T-C

64816659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93054310-C-G

64816659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93054310-C-T

64816735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93054378-T-C

64816769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93054415-G-A

64816845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93054491-T-C

64823511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056560-C-T

64823599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056634-A-T

64823610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056645-A-T

64823661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93056690-A-G

64824446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058159-C-G

64824503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058218-C-G

64824503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058218-C-T

64824561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058274-A-G

64824591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058304-T-A

64824634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93058344-C-T

64824706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058416-T-C

http://identifiers.org/hco/3/GRCh38#64824804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93058506-A-C

64824804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058506-A-G

64824850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058553-C-T

http://identifiers.org/hco/3/GRCh38#64824912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93058613-A-C

http://identifiers.org/hco/3/GRCh38#64825103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93058803-C-A

64825293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93058981-C-T

64825525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93059206-T-C

http://identifiers.org/hco/3/GRCh38#64825544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93059221-C-A

64825587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93059263-G-C

64825670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93059332-C-T

64825843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93059491-C-T

64826076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93059720-C-T

64828430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93060851-A-G

64828744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93061132-A-G

64828867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93061236-A-G

64829636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93061906-G-T

64830470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93062680-C-T

64830483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93062693-G-A

64830483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93062693-G-C

64830813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063008-T-C

64830815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063010-G-C

64830879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063074-G-T

http://identifiers.org/hco/3/GRCh38#64830993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93063184-C-A

64831048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063240-C-T

64831114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063306-C-G

64831114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063306-C-T

64831284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93063471-A-G

http://identifiers.org/hco/3/GRCh38#64831534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93063694-A-C

http://identifiers.org/hco/3/GRCh38#64832658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93064878-C-A

64832658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93064878-C-G

64832815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93065060-G-A

64832815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93065060-G-T

64832855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93065102-A-G

64832855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93065102-A-T

64833029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93065364-C-G

64833029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93065364-C-T

64833705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93066089-G-C

64833757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93066268-C-T

64833920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93066396-G-A

64834182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93066662-G-A

64834523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93066986-G-C

http://identifiers.org/hco/3/GRCh38#64834609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93067074-C-A

64834609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93067074-C-G

64834670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93067124-A-G

64834691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93067138-G-T

64834703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93067150-G-T

http://identifiers.org/hco/3/GRCh38#64834716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93067163-C-A

64835017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93068418-T-C

64835225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93068765-G-T

64835350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93068868-T-C

64835350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93068868-T-G

64835474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93068983-C-T

http://identifiers.org/hco/3/GRCh38#64835475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93068984-A-C

64835475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93068984-A-T

64835639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93069127-C-T

64835727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93069218-T-C

64836482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93069677-A-G

64836596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93069779-T-C

64836640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93069830-T-C

64836975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93070591-A-G

64837066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93070654-G-A

64837066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93070654-G-C

64837184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93070748-T-C

64837248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93070812-C-G

64837258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93070818-T-G

http://identifiers.org/hco/3/GRCh38#64837299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93070859-C-A

64837299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93070859-C-T

http://identifiers.org/hco/3/GRCh38#64837353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93070911-C-A

64837353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93070911-C-T

64837550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93071088-T-G

64837604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93071137-G-A

64837604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93071137-G-T

64837709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93071237-G-A

64838085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93071637-A-G

64838085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93071637-A-T

64838126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93071678-G-A

64838238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93071775-A-G

64838252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93071789-G-A

64838795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072320-C-T

http://identifiers.org/hco/3/GRCh38#64840005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93074165-A-C

64840071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93074227-T-A

64840118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93074272-T-G

64840156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93074299-A-T

64840164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93074307-C-T

64840220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93074361-T-C

64840486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93074619-C-T

64840668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93074796-G-C

64840726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93074854-G-A

64840726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93074854-G-T

64840890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93075010-G-A

64840960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93075075-C-G

64841716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93077133-G-C

64842205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93077275-T-C

64842382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93077420-G-A

64843122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083895-T-C

64843122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083895-T-G

64843184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083957-A-G

64843602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084583-C-T

64843875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084875-G-A

64844160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085156-G-A

64844252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085242-C-T

64845074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085559-A-G

64845083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085568-C-G

64845270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085797-T-C

http://identifiers.org/hco/3/GRCh38#64845309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93085833-A-C

64845309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085833-A-G

64845347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085869-C-G

64845377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085899-C-T

http://identifiers.org/hco/3/GRCh38#64845668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93086154-C-A

64845668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93086154-C-T

64845711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93086190-G-A

64845711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93086190-G-T

64845730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93086208-G-A

http://identifiers.org/hco/3/GRCh38#64846071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93086513-C-A

64846994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93087413-T-C

64847207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93087595-C-T

64847235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93087621-T-C

http://identifiers.org/hco/3/GRCh38#64847253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93087639-C-A

64848202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93089616-G-A

64848247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93089660-T-C

64848735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93090189-A-T

64848850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93090319-A-G

64848959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93090426-C-T

64849516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93090732-T-G

64849522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93090738-A-T

64849535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93090751-A-G

64849584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93090800-A-G

http://identifiers.org/hco/3/GRCh38#64849606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93090823-C-A

http://identifiers.org/hco/3/GRCh38#64849685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93090879-C-A

64851398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93092192-A-G

64851497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93092274-C-T

64851635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93092400-T-C

64851933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93092688-G-A

64852219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93092968-G-T

64852585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93093316-A-G

http://identifiers.org/hco/3/GRCh38#64852715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93093433-C-A

64852995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93093711-G-C

64853179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93093894-G-A

64853316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93094020-T-C

64853316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93094020-T-G

64853511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93094215-A-G

64853934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93094588-G-T

64853961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93094611-A-G

64854372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095003-C-G

64854372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095003-C-T

64854373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095004-C-T

64854391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095020-G-A

64854462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095076-G-A

64854573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095182-G-C

64854583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095192-T-G

64854605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095211-A-G

64854621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095227-G-A

64855008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095549-G-A

64855045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095586-C-T

64855129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095657-C-T

64855153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095675-A-G

http://identifiers.org/hco/3/GRCh38#64855689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93096370-A-C

64855839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93096520-C-T

64855873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93096547-A-G

http://identifiers.org/hco/3/GRCh38#64856085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93096756-C-A

64856805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93097653-C-T

http://identifiers.org/hco/3/GRCh38#64856932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93097772-A-C

64857046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93097892-G-C

64857214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93098063-A-G

64857509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93098349-G-A

64857509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93098349-G-C

64857524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93098363-C-T

64859642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101092-A-G

64859780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101193-G-A

64860060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101494-G-A

http://identifiers.org/hco/3/GRCh38#64860296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93101722-C-A

64860308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101734-A-T

64860338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101764-A-T

64860473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101902-G-C

64860609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93102128-G-C

64861137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93102748-T-G

64861163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93102773-T-C

64861364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93102948-G-A

64861364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93102948-G-T

http://identifiers.org/hco/3/GRCh38#64861381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93103679-C-A

64861381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103679-C-T

64862015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93104234-G-T

64862057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93104277-G-A

64862226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93104400-T-C

64862262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93104429-C-T

64862635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93104592-A-T

http://identifiers.org/hco/3/GRCh38#64862937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93104850-C-A

64863292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93105198-A-G

64863376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93105550-C-T

http://identifiers.org/hco/3/GRCh38#64863378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93105552-C-A

64863577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93105778-T-C

64863606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93105809-T-C

64863855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93106217-T-C

64863900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93106259-A-G

64864208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93106560-T-C

64864329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93106680-A-G

64864674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107023-C-T

64864684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107033-C-T

64864820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107155-C-T

64864876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107208-C-T

64864910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107239-A-G

64865036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107373-G-A

64865201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107534-G-A

64865201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107534-G-C

64865618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107691-T-C

http://identifiers.org/hco/3/GRCh38#64866011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93107997-C-A

64866011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107997-C-T

64866231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93108260-G-T

64867602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109677-A-T

64868179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93110288-C-T

64868458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93111956-G-A

http://identifiers.org/hco/3/GRCh38#64868857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93112292-A-C

64869854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93113554-A-G

64869855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93113555-T-A

64869935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93113635-T-A

64869945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93113641-G-A

64869945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93113641-G-T

http://identifiers.org/hco/3/GRCh38#64870053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93113727-A-C

64870360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93115536-G-T

64870426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93115602-G-T

64870584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93115734-G-A

64871249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93116828-T-A

64871439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117022-T-C

http://identifiers.org/hco/3/GRCh38#64871591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93117172-C-A

64871703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117255-T-G

64871736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117265-T-C

64871753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117282-G-A

64871753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117282-G-C

64871753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117282-G-T

64871863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117392-G-A

64871863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117392-G-T

64871914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117477-T-G

64872032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117581-T-C

64872288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117831-G-A

64872382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117925-G-A

64872554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118090-C-G

64872606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118122-A-G

64872660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118176-G-T

64872773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118254-C-T

64874434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118807-A-G

64874434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118807-A-T

64874616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118977-G-A

64874616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118977-G-T

64875429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93119833-T-C

64875517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93119913-G-T

64875659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93120052-C-T

http://identifiers.org/hco/3/GRCh38#64875733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93120128-C-A

64875763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93120157-G-A

64875770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93120164-T-C

64875795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93120189-G-A

64876205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93120287-A-G

64876384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93120453-A-G

64876425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93120494-C-T

64876426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93120495-G-A

64876480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93120544-A-G

http://identifiers.org/hco/3/GRCh38#64876548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93120609-C-A

http://identifiers.org/hco/3/GRCh38#64876636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93121301-C-A

64876774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93121430-T-C

64876821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93121484-A-G

64876906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93121568-T-C

64877010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93121656-C-T

64877061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93121707-A-G

64877139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93121784-G-A

64877243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93121876-G-A

64877283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93121911-A-G

64877287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93121915-T-C

64877349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93121968-A-G

64877523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93122128-G-A

64878592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93122384-C-T

http://identifiers.org/hco/3/GRCh38#64878745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93122545-A-C

64878771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93122566-T-C

64878852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93122647-T-A

64878852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93122647-T-C

64878924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93122716-A-G

http://identifiers.org/hco/3/GRCh38#64878954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93122746-A-C

64879110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93122889-T-C

64879986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93123547-T-C

64882069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93123901-G-A

64882394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93124148-C-T

64882395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93124149-T-A

64882402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93124156-C-G

64882402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93124156-C-T

64882670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93125041-C-T

64882846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93125223-C-G

64883051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93125424-G-A

64883220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93125581-A-T

64883430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93126348-G-A

64883430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93126348-G-T

64883588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93126509-A-T

64883625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93126534-G-A

64883726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93126612-A-T

64884311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93127294-G-A

64884311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93127294-G-C

64884366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93127343-A-G

64884493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93127473-T-C

http://identifiers.org/hco/3/GRCh38#64884510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93127490-C-A

64884511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93127491-T-C

64884650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93127642-C-T

64884895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93127855-T-C

64885190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128145-T-C

64885284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128237-T-C

http://identifiers.org/hco/3/GRCh38#64885341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93128276-C-A

64885367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128297-C-T

64885374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128304-C-G

64885374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128304-C-T

64885404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128334-A-G

64885404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128334-A-T

64885558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128368-T-C

64885713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128446-T-G

64885716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128449-T-C

64885731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128464-C-G

http://identifiers.org/hco/3/GRCh38#64886021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93128603-A-C

64886021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128603-A-G

64886245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128746-T-G

64886247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128748-T-C

64886346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93128831-C-T

64886665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93129260-T-C

64886757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93129351-A-G

64886776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93129370-G-A

64886776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93129370-G-C

http://identifiers.org/hco/3/GRCh38#64886817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93129406-C-A

http://identifiers.org/hco/3/GRCh38#64886967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93129557-C-A

64887466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93129724-T-C

64887603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93129840-C-T

64887957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130075-C-G

64888122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130162-A-G

http://identifiers.org/hco/3/GRCh38#64888882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93130634-C-A

64888895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130648-T-A

64888943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130700-T-G

64888999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130767-A-G

64889112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130886-C-G

64889261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93131016-G-A

64889282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93131057-G-C

64889344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93131103-C-T

http://identifiers.org/hco/3/GRCh38#64889963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93131387-C-A

64890113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93131522-C-T

http://identifiers.org/hco/3/GRCh38#64890173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93131582-C-A

64890173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93131582-C-T

64890196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93131608-G-A

64890334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93131751-G-A

64890460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93132284-T-A

64890737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93132570-A-T

64890902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93133036-G-C

64890972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93133128-A-G

64891016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93133161-G-T

http://identifiers.org/hco/3/GRCh38#64891109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93133253-A-C

64891316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93133424-T-A

64891316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93133424-T-G

64891321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93133429-G-A

64891321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93133429-G-T

http://identifiers.org/hco/3/GRCh38#64891332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93133440-C-A

64891332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93133440-C-T

64892322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134064-G-C

64892660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134284-G-T

64892662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134286-C-T

http://identifiers.org/hco/3/GRCh38#64892848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93134446-C-A

64893216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134753-C-G

64893272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134795-T-G

64893465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134962-T-C

http://identifiers.org/hco/3/GRCh38#64893569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93135061-C-A

64893569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93135061-C-T

64893718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93135195-G-T

64893801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93135273-T-G

http://identifiers.org/hco/3/GRCh38#64893999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93135503-C-A

64894249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93135747-G-A

64894281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93135780-G-A

64894488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93135969-G-A

64894869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93136321-C-G

64895151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93136608-A-T

64895166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93136623-T-C

http://identifiers.org/hco/3/GRCh38#64895347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93136810-C-A

64896099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93137484-G-A

64896466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93139081-G-A

64897028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93139586-G-A

64897764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93140820-T-C

64897786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93140844-G-T

64898584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93142030-G-A

64898624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93142070-G-C

64898806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93142212-A-T

64898826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93142232-A-G

64898899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93142293-A-G

64898941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93142332-A-T

64900098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93142844-G-A

64900098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93142844-G-T

64900105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93142851-G-A

http://identifiers.org/hco/3/GRCh38#64900123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93142869-C-A

64900409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93143131-G-C

64900686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93143404-C-T

64900893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93143667-G-A

64901263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93143991-A-G

64901296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93144012-T-C

64901515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93144228-G-T

http://identifiers.org/hco/3/GRCh38#64901550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93144264-C-A

64901825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93144543-A-G

64902045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93144757-T-G

64902207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93144894-C-G

64902364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93144986-G-A

64902394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93145018-A-G

http://identifiers.org/hco/3/GRCh38#64902612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93145176-C-A

64902899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93145472-G-C

64903069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93145642-G-A

64903081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93145654-T-C

64903154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93145727-C-T

64903289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93145862-G-A

64903503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93146069-G-A

64903753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93146783-G-A

64903809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93146827-C-T

64903882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93146898-C-T

64904018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93147012-C-T

64904062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93147507-T-C

64904172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93147614-A-G

64904398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93147854-C-T

http://identifiers.org/hco/3/GRCh38#64904517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93147968-C-A

http://identifiers.org/hco/3/GRCh38#64905064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93148197-A-C

64905189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93148340-C-G

64905244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93148398-G-A

http://identifiers.org/hco/3/GRCh38#64905345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93148495-C-A

64905346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93148496-C-T

64905382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93148532-T-C

64905477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93148591-T-C

http://identifiers.org/hco/3/GRCh38#64905499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93148613-C-A

64905548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93148656-C-G

64905610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93148722-C-T

64905629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93148745-T-A

64905799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93148919-C-T

64905823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93148943-T-A

64905823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93148943-T-C

64905844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93148964-T-C

64906167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93149254-A-G

64906262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93149345-G-A

64906289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93149371-C-T

64906530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93149616-A-T

64906543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93149629-A-G

64906629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93149698-G-A

64906651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93149722-G-A

64907029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93150385-C-T

64907115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93150466-T-C

64907182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93150539-C-T

64907223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93150580-T-G

64907306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93150660-G-C

64907415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93150752-C-T

64907454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93150799-T-A

64907467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93150812-G-A

64907483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93150828-T-C

64907483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93150828-T-G

64907554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93150916-T-A

64907623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93150990-G-C

64907914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93151397-A-G

64908044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93151523-C-G

64908146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93151629-G-A

64908261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93151734-G-A

64908261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93151734-G-C

http://identifiers.org/hco/3/GRCh38#64908310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93151783-C-A

64908523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93151991-G-A

64908906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93152374-G-T

64908942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93152410-G-A

64908942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93152410-G-T

64909091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93153244-G-A

64909194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93153380-C-G

64909195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93153381-T-C

64909251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93153435-A-G

http://identifiers.org/hco/3/GRCh38#64909314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93153487-C-A

64909314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93153487-C-G

64909314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93153487-C-T

64909522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93153695-T-C

64909628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93153813-G-A

64909807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93154039-T-C

64909811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93154043-T-C

64909818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93154050-A-G

64909818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93154050-A-T

64909820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93154052-T-C

64909886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93154120-C-T

64909977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93154219-G-A

64909977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93154219-G-C

64910016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93154261-G-A

64910026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93154268-G-A

64910197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93154420-T-A

64910270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93154487-C-T

http://identifiers.org/hco/3/GRCh38#64910318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#93154533-C-A

64910704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93154908-A-G

64910724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93154928-G-A

64910787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93154989-G-T

64910823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93155028-T-C

64911028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93155235-C-T

http://identifiers.org/hco/3/GRCh38#64911093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93155292-C-A

64911093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93155292-C-T

64911138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93155335-T-C

64911181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93155379-A-G

64911304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93155515-C-T

64911305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93155516-G-A

64911406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93155662-A-G

64911411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93155667-A-G

64911467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93155758-G-A

64911638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93156180-T-G

64911791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93156344-T-C

64913211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93156938-G-A

64913244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93156971-C-T

64913278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93156997-G-A

64913386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93157131-G-A

64913389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93157134-G-A

http://identifiers.org/hco/3/GRCh38#64914165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93158056-C-A

64914209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93158093-T-C

http://identifiers.org/hco/3/GRCh38#64914213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93158097-C-A

http://identifiers.org/hco/3/GRCh38#64914247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93158272-A-C

64914498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93158534-G-A

64914588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93158658-C-T

64914618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93158688-T-C

64914717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93158763-A-G

64914880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93158859-G-A

64914880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93158859-G-C

64915649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93160416-G-A

64915649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93160416-G-T

64915720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93160483-G-A

64916070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93160829-A-G

64916195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93160955-G-A

64916393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161153-C-T

64916587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161336-G-C

64916651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161403-A-T

64916689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161444-T-C

64916707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161460-G-A

64916915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161643-T-G

64917009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161733-A-G

64917176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161900-G-A

64917176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161900-G-C

64917193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161923-A-G

64917196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161926-G-T

64917225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161961-A-G

64917816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93165975-G-A

64917865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93166033-C-T

64917943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93166106-T-C

64917968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93166131-T-C

64918126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93166288-T-C

http://identifiers.org/hco/3/GRCh38#64918149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93166311-A-C

64918181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93166343-A-G

64918858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93166650-A-G

http://identifiers.org/hco/3/GRCh38#64918871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93166661-A-C

64918952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93166740-T-A

64919410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93167780-C-G

64919481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93167841-G-T

64919752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93168378-T-A

http://identifiers.org/hco/3/GRCh38#64919768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93168394-C-A

64919869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93168481-C-T

64920184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93168736-T-C

64920586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93169937-G-A

64920586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93169937-G-C

64920599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93169950-T-A

64920618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93170003-G-C

64920670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93170056-C-G

64920681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93170067-T-C

64920869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93170235-G-A

64920968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93170339-C-T

64921004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93170372-C-T

64921038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93170403-G-C

64921592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93170984-T-C

64921632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93171022-A-G

64921692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93171078-G-A

64922017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93171661-C-T

64922095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93171715-T-G

64922143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93171763-C-G

64922222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93171839-G-C

64922222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93171839-G-T

64922288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93171946-T-A

64922440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93172085-C-G

64922467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93172111-G-T

64922572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93172203-T-A

64923083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93173044-C-T

64923226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93173207-T-C

http://identifiers.org/hco/3/GRCh38#64923408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93173397-C-A

64924317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93174403-G-A

64924317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93174403-G-T

64924600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93174704-G-T

64924678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93174782-A-G

64924697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93174801-C-T

64924811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93174914-C-T

64925004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93175133-T-C

64925342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93175636-G-C

64925587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93175919-G-A

64925822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93176144-C-T

64925861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93176178-G-T

64925880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93176196-T-A

64926121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93176412-A-G

64926930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93176867-G-A

64926994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93176919-T-A

64926994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93176919-T-C

64927302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93177246-A-G

http://identifiers.org/hco/3/GRCh38#64927401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93177336-C-A

64927505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93177424-A-G

64927726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93177889-A-G

http://identifiers.org/hco/3/GRCh38#64927768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93177932-C-A

http://identifiers.org/hco/3/GRCh38#64927856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93178014-C-A

64928070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93178253-C-T

64928137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93178286-T-A

64928497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93178358-G-A

64928538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93178399-T-C

64928693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93178554-C-T

64928730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93178593-G-A

64928833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93178696-A-G

64928997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93178865-T-C

64929086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93178955-G-C

64930862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93184668-T-A

64931005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93184810-T-C

64931072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93184963-T-C

64931105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93185001-G-A

64931223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93185093-G-A

http://identifiers.org/hco/3/GRCh38#64931224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93185094-A-C

64931275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93185172-A-G

64931431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93185298-T-A

64931441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93185308-T-C

64931526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93185382-C-T

64931629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93185480-A-T

64931743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93185589-C-G

64931837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93185677-C-T

64931997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93185841-A-G

64932062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93185887-G-A

64932110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93185927-T-A

64932110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93185927-T-C

64932620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186706-A-G

64933380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186861-G-A

64933399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186879-T-C

64933419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93186899-T-C

http://identifiers.org/hco/3/GRCh38#64933541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93187025-A-C

64934326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93187493-C-T

64934682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93189762-A-G

64934682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93189762-A-T

64934701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93189781-T-C

http://identifiers.org/hco/3/GRCh38#64934765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93189852-A-C

64935059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190097-A-T

64935073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190111-C-G

64935080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190118-T-C

64935138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190161-C-T

64935143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190166-C-T

64935529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190370-A-G

64935564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190403-A-G

64935566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190405-C-T

http://identifiers.org/hco/3/GRCh38#64935569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93190408-C-A

64935569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190408-C-T

64935570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190409-G-A

64935583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190422-C-T

64935694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190531-T-C

64935835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93190664-G-T

http://identifiers.org/hco/3/GRCh38#64935986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93190776-A-C

64936531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93191330-C-G

64936542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93191341-T-C

64936588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93191388-T-C

64936590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93191390-G-T

64936652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93191453-G-A

64936673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93191474-C-G

http://identifiers.org/hco/3/GRCh38#64936731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93191522-A-C

64936763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93191552-G-C

64936858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93191645-G-A

64936881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93191668-G-A

http://identifiers.org/hco/3/GRCh38#64936930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93191705-A-C

http://identifiers.org/hco/3/GRCh38#64936956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93191733-C-A

http://identifiers.org/hco/3/GRCh38#64937105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93191864-A-C

64937265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93192000-T-C

64937476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93192261-G-A

64937503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93192288-T-A

64937503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93192288-T-C

64937598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93192415-G-A

64938191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193200-A-G

64938315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193316-T-A

64938315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193316-T-C

64938315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193316-T-G

http://identifiers.org/hco/3/GRCh38#64938378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93193379-A-C

64938378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193379-A-G

64938414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193414-G-T

64938516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193484-T-C

64938680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193651-A-T

64938691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193662-C-T

64938774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193737-C-G

64938826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193792-G-A

64938921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193869-C-T

64938938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193886-T-C

64938952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93193900-A-G

http://identifiers.org/hco/3/GRCh38#64938994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93193941-C-A

64939075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93194000-G-T

64939080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93194005-A-G

64939137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93194067-T-C

64940707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93195490-T-A

64940707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93195490-T-C

http://identifiers.org/hco/3/GRCh38#64940739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93195524-C-A

64940877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93195656-C-T

64940891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93195670-C-T

64940956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93195736-G-A

64941038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93195818-A-T

http://identifiers.org/hco/3/GRCh38#64941054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93195834-C-A

64941054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93195834-C-T

64941334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93196087-A-G

64941657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93196337-T-C

64941660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93196340-G-A

64941678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93196358-C-T

64941734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93196438-C-T

64941749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93196453-C-T

64941823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93196521-C-T

64941886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93196602-C-T

64941945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93196663-T-A

http://identifiers.org/hco/3/GRCh38#64942026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93196730-A-C

64942026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93196730-A-G

http://identifiers.org/hco/3/GRCh38#64942085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93196784-A-C

64942250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93196950-A-G

64942250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93196950-A-T

64942566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93198015-G-C

64942620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 93198071-C-T

64942732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93198169-T-C

64942841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93198249-G-A

64942843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93198251-T-C

64942845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93198253-C-T

http://identifiers.org/hco/3/GRCh38#64942870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93198278-C-A

64942887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93198292-A-G

64942898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93198303-G-T

64943201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93198608-G-A

64943330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93198733-G-A

64943477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93198887-C-T

64943631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199050-G-A

64943635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199054-G-A

64943666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199085-C-T

64943667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199086-T-C

64943715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199124-G-A

http://identifiers.org/hco/3/GRCh38#64943963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93199484-C-A

64943976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199496-G-A

http://identifiers.org/hco/3/GRCh38#64944120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93199944-A-C

64944146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199970-T-C

64944146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93199970-T-G

64944219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93200050-T-C

64944239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93200070-C-G

64944291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93200098-G-A

64944383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93200213-C-T

64944479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93200332-A-G

64944541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93200385-G-T

64944665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93200469-T-G

64945114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93200886-T-C

64945203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93200977-G-C

64945560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93201342-C-T

64945567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93201354-T-A

64945581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93201369-G-A

64945581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93201369-G-C

64945618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93201418-G-C

64945663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93201463-G-A

64945772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93201567-T-G

64945799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93201573-C-T

64945902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93201640-C-T

64946003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93201741-C-T

64946022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93201760-A-G

64946025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93201763-G-A

64946801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93203071-G-C

64947641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93203790-G-A

64947661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93203819-G-C

64947898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93204013-C-T

http://identifiers.org/hco/3/GRCh38#64947917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93204021-A-C

64948161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93204168-G-A

http://identifiers.org/hco/3/GRCh38#64949998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93206867-C-A

64950022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93206892-T-C

64950057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93206929-T-C

64950065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93206937-G-A

64950144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93207016-C-T

64950221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93207099-T-G

64950499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93207414-C-G

64951001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208237-G-A

64951016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208252-C-G

64951357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208499-A-T

64951422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208563-T-C

64951503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93208636-C-G

64951640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93209076-G-A

http://identifiers.org/hco/3/GRCh38#64951691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93209123-C-A

http://identifiers.org/hco/3/GRCh38#64951710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93209142-C-A

64951719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93209151-C-G

64951921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93209332-T-C

64951941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93209352-G-A

64954866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93209532-C-G

64954914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93209585-G-A

64954995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93209665-G-A

64955169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93209845-C-T

64955241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93209917-C-T

http://identifiers.org/hco/3/GRCh38#64955283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93209959-A-C

64955283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93209959-A-G

64955801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93210498-A-G

64955991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93210664-T-C

64956300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93210938-T-A

64956335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93210973-C-T

64956673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93211663-T-C

64956730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93211720-C-G

64956752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93211742-G-A

64956985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93211971-G-A

http://identifiers.org/hco/3/GRCh38#64957173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93212154-C-A

64957173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93212154-C-T

64957221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93212200-C-G

64957273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93212255-T-A

64957273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93212255-T-C

64957327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93212309-A-G

64957335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93212317-G-C

64957335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93212317-G-T

http://identifiers.org/hco/3/GRCh38#64957606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93212647-A-C

http://identifiers.org/hco/3/GRCh38#64957661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93212703-C-A

http://identifiers.org/hco/3/GRCh38#64957717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93212758-A-C

64957927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93212975-C-T

64957938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93212986-C-G

64958096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93213146-T-C

64958145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93213201-T-C

64958313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93213370-G-C

64958541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93213549-T-C

64958625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93213674-A-G

64958874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93214101-A-G

64959381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93214816-G-A

64959393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93214828-G-A

64959521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93214959-G-T

64959636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93215075-G-A

64959636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93215075-G-T

http://identifiers.org/hco/3/GRCh38#64959684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93215123-C-A

64959684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93215123-C-T

64959802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93215244-T-C

64959834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93215276-T-C

64960248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93215696-T-C

64960641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93216019-T-C

64961377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93216934-C-T

http://identifiers.org/hco/3/GRCh38#64961606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#93217139-A-C

64961634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93217167-G-T