78000176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104164344-T-A

78000176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104164344-T-C

78000356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104164492-G-T

78006666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104164701-A-G

http://identifiers.org/hco/13/GRCh38#78006745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104164756-C-A

78006771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104164766-C-T

78006772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104164767-A-G

78006922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104164898-T-G

78006948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104164922-C-T

78006973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104164961-T-A

78007078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104165057-T-A

http://identifiers.org/hco/13/GRCh38#78007179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104165135-C-A

78007179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104165135-C-T

78007484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104167247-G-C

78008203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104167944-C-T

78008222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104167963-C-G

78008222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104167963-C-T

78010359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104168970-C-G

78010359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104168970-C-T

78010389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104168994-G-T

78010404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104169009-T-C

78010450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104169055-T-C

78010483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104169088-C-T

78010519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104169115-C-T

78010554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104169150-T-G

78010589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104169185-A-G

78010635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104169239-T-C

78010986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104169986-A-G

78011011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104170012-G-A

78011229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104170219-A-G

78011466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104170445-T-G

78013086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104170968-G-T

78013088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104170970-G-T

78013136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104171016-C-T

78013224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104171105-T-G

78013342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104171227-T-C

78013342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104171227-T-G

78013629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104171490-G-T

78013630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104171491-C-G

78019386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104175636-A-G

78019485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104175732-G-A

78019506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104175755-G-T

78019535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104175785-G-C

78019728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104175956-A-T

78019785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104176006-G-T

78019836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104176059-T-C

78019851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104176074-T-G

78019874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104176076-T-A

78019900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104176102-A-G

78019900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104176102-A-T

78020687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104177170-G-A

78020690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104177173-G-A

78020690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104177173-G-C

78020744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104177235-A-G

78020850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104177340-G-A

78020918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104177409-C-G

78020918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104177409-C-T

78020931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104177422-C-T

http://identifiers.org/hco/13/GRCh38#78021218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104177690-C-A

78021218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104177690-C-T

78021254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104177726-T-C

78021485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104177946-G-T

78021585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104178030-T-C

78021585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104178030-T-G

78021773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104178413-T-C

78021821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104178457-A-T

78021921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104178566-T-C

78022100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104178724-G-A

78022131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104178754-G-T

78022134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104178757-G-A

78022146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104178769-C-T

78022147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104178770-G-A

78022257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104178890-G-A

78022376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104178998-T-G

78022391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104179007-C-G

78022391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104179007-C-T

http://identifiers.org/hco/13/GRCh38#78022481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104179024-C-A

78022574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104179106-T-A

78022633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104179158-G-A

78022668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104179209-A-G

78022700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104179241-C-T

78025437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104182811-G-T

78025499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104182868-T-C

78025528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104182896-C-T

78025560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104182928-A-G

78025597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104182965-C-T

78025661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104183030-C-T

78025666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104183034-A-G

http://identifiers.org/hco/13/GRCh38#78025689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104183054-C-A

78025771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104183139-G-T

78025783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104183154-C-T

78026283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104183620-T-G

78029519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104185031-A-G

78029563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104185083-T-C

78029635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104185218-G-A

78029663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104185239-A-G

78029741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104185304-C-T

http://identifiers.org/hco/13/GRCh38#78029830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104185381-A-C

78029830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104185381-A-T

78029949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104185500-G-A

78029949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104185500-G-C

78029949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104185500-G-T

78029963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104185514-G-A

78030034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104185579-A-G

78030224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104185762-G-T

78030226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104185764-A-G

78030227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104185765-T-C

78030245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104185782-A-G

78030245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104185782-A-T

http://identifiers.org/hco/13/GRCh38#78030292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104185828-C-A

78030292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104185828-C-T

78030293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104185829-G-A

78030293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104185829-G-T

http://identifiers.org/hco/13/GRCh38#78030750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104186145-C-A

78030759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104186154-C-G

78031101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104186470-T-C

78031315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104186663-G-A

78031351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104186700-G-A

78031394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104186736-C-G

78031844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104187105-A-G

78031871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104187132-A-G

78032587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104187836-T-A

78032683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104187928-G-T

78034280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104189801-T-C

78034333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104189860-T-C

78034408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104190026-G-A

78034477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104190103-T-A

78034477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104190103-T-C

78034576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104190198-A-G

78034790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104192012-T-C

78034892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104192069-G-C

78034912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104192089-G-C

78034931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104192103-C-T

78034970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104192142-A-G

78035115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104192311-T-A

78035116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104192312-T-C

78035303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104192485-T-C

78035354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104192537-A-G

78035909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104193430-G-A

78035910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104193431-G-T

78035985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104193504-G-T

http://identifiers.org/hco/13/GRCh38#78036032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104193535-A-C

78036046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104193550-G-A

78036206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104193761-A-G

78036629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104194121-A-G

78036711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104194173-G-T

http://identifiers.org/hco/13/GRCh38#78036733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104194191-C-A

78036738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104194194-T-A

78036760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104194214-C-T

78039038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104194579-G-C

78039067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104194609-C-T

78039076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104194618-T-A

http://identifiers.org/hco/13/GRCh38#78039115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104194657-C-A

78039219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104194761-T-C

78042410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104198604-T-C

78042443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104198633-T-C

78042465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104198652-T-C

78042500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104198687-T-A

78042522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104198709-C-T

78042878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104199142-A-G

78042889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104199153-T-C

78042940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104199191-G-T

78042945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104199197-G-A

http://identifiers.org/hco/13/GRCh38#78043136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104199395-A-C

78043191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104199441-A-G

78043721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104199891-G-A

78043948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104200090-C-T

78043983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104200123-T-C

78043986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104200126-G-A

78044133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104200254-T-G

78044229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104200696-T-A

http://identifiers.org/hco/13/GRCh38#78044468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104200946-A-C

78044468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104200946-A-G

78044543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104201746-T-A

78044543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104201746-T-G

78044554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104201757-A-G

78044687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104201885-T-C

78044761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104201960-C-T

78044911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104202092-A-G

78044920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104202101-A-G

78045516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104202968-A-G

78045659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104203093-G-T

78045981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104203390-C-G

78046334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104203908-G-A

78046334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104203908-G-C

78046334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104203908-G-T

http://identifiers.org/hco/13/GRCh38#78046374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104203939-C-A

78046379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104203944-G-A

78046435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104203997-T-A

78046435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104203997-T-C

78046544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104204103-G-C

78050387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104206419-G-A

78050387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104206419-G-C

78050387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104206419-G-T

78050478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104206507-T-A

78050478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104206507-T-C

http://identifiers.org/hco/13/GRCh38#78051068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104207191-C-A

http://identifiers.org/hco/13/GRCh38#78051116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104207246-C-A

78052520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104207533-T-A

http://identifiers.org/hco/13/GRCh38#78052550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#104207563-A-C

78052608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104207616-A-T

78052610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104207618-G-A

78052979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104208009-T-A

78052979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104208009-T-G

78053326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104208274-G-A

78053326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104208274-G-T

78053388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104208334-G-A

78053388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104208334-G-T

78053451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104209122-T-C

78053453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104209124-T-G

78053477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 104209150-G-T

78053483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42783
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104209155-C-T