67327036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94242812-G-T

67327111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94242883-G-T

http://identifiers.org/hco/13/GRCh38#67327146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94242918-C-A

http://identifiers.org/hco/13/GRCh38#67327239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94243017-C-A

67327239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94243017-C-T

67327379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94243167-T-C

67328779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94244921-T-C

67328923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94245054-C-T

67329451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94245563-C-T

67329482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94245592-G-A

67329482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94245592-G-C

67330298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94254452-G-A

67330528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94254679-A-G

67330533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94254684-C-G

67330773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94254839-G-A

67330838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94254904-A-G

67330845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94254911-A-G

67331145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94255206-G-C

http://identifiers.org/hco/13/GRCh38#67331200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94255261-A-C

67331495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94255543-A-G

67331701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94255740-C-G

67332668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94257403-T-G

http://identifiers.org/hco/13/GRCh38#67333618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94257635-C-A

67333742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94257765-A-T

67334337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94258513-A-G

67334337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94258513-A-T

http://identifiers.org/hco/13/GRCh38#67334631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94258695-C-A

http://identifiers.org/hco/13/GRCh38#67334651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94258715-C-A

67334656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94258720-T-C

67334668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94258726-C-T

67334780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94258802-G-A

67334947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94258966-G-T

67334952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94258971-C-T

67334963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94258980-T-A

67335075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94259085-A-G

67336228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94260675-G-A

67336631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94261054-A-G

67336686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94261133-A-G

67336787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94261217-T-C

67336787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94261217-T-G

67336859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94261464-C-T

67337008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94261559-T-G

http://identifiers.org/hco/13/GRCh38#67337037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94261592-C-A

67337116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94261678-T-C

67348629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94263140-T-C

67348664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94263158-T-C

67348881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94263345-G-A

67348931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94263395-T-C

67349134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94263594-T-C

67349168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94263628-G-A

67351169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94263810-T-A

67351169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94263810-T-G

67351182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94263823-T-C

67351399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94264042-A-G

67351399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94264042-A-T

http://identifiers.org/hco/13/GRCh38#67351460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94264100-A-C

http://identifiers.org/hco/13/GRCh38#67353053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94264780-A-C

67353543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94265411-G-A

67353543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94265411-G-T

67353545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94265413-T-C

67353661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94265525-G-A

67353745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94265608-T-A

67353769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94265631-C-T

http://identifiers.org/hco/13/GRCh38#67353853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94265716-C-A

67353853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94265716-C-T

67353886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94265748-A-G

67353952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94265809-G-A

67354157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94266024-G-T

67354166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94266033-A-T

67354299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94266149-C-T

67354335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94266182-G-A

67354335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94266182-G-C

67354387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94266233-G-A

67354465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94266324-G-A

67355137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94271459-A-G

67355139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94271461-G-A

67355145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94271468-G-A

67355145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94271468-G-C

67355275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94271600-A-G

67355320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94272594-A-G

67355390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94272663-A-T

67355458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94272727-T-C

67355458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94272727-T-G

67355497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94272758-G-T

67355520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94272782-G-A

67355598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94272857-C-T

67355600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94272859-C-T

67355837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94273253-G-A

67356424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94273840-A-T

67356554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94273975-T-G

http://identifiers.org/hco/13/GRCh38#67356575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94273996-C-A

67356794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274184-T-C

http://identifiers.org/hco/13/GRCh38#67356824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94274213-C-A

67356835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274224-C-G

67356835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274224-C-T

http://identifiers.org/hco/13/GRCh38#67356847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94274236-A-C

67356847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274236-A-G

67356860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274249-A-G

67356916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274305-G-T

67356934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274321-C-T

67356973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274347-C-T

67356984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274358-G-A

67357139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274483-G-A

67357139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274483-G-T

67357300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274635-G-T

67357550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274857-C-T

67357626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274937-G-A

67357626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94274937-G-T

http://identifiers.org/hco/13/GRCh38#67357697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94275008-C-A

67357697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94275008-C-G

67358107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94275095-G-A

67358201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94275184-G-A

67358357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94275331-A-T

67358458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94275430-A-G

67358831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94275811-C-T

67358848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94275828-C-G

67358848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94275828-C-T

67358984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94275961-T-C

67359062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276034-T-A

http://identifiers.org/hco/13/GRCh38#67359142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94276114-C-A

67359142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276114-C-T

http://identifiers.org/hco/13/GRCh38#67359205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94276176-C-A

67359221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276192-G-A

67359346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276317-G-A

67359360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276335-C-T

67359445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276407-T-C

67359483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276445-C-T

67359727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276625-A-T

67359779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276681-A-T

67359857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276764-T-A

67359858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276765-C-T

67359862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276770-G-A

67359983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276864-T-C

67359993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276874-T-C

67360149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276972-G-A

67360186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94276996-A-T

67360242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94277039-C-T

67360506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94277289-A-G

67360607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94277371-A-G

67360670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94277434-T-C

http://identifiers.org/hco/13/GRCh38#67363963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94277630-C-A

67364114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94277776-G-A

67364285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94277940-T-C

67364428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94278072-A-G

67364599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94278245-T-C

67364605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94278251-C-T

67365276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94278511-A-G

67365293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94278528-A-G

http://identifiers.org/hco/13/GRCh38#67365471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94278699-C-A

67365471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94278699-C-G

http://identifiers.org/hco/13/GRCh38#67365509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94278717-A-C

67365509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94278717-A-G

http://identifiers.org/hco/13/GRCh38#67365775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94278955-A-C

67367430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94280361-G-A

67367553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94280485-G-T

67367563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94280495-G-C

67367725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94280638-G-A

67367914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94280806-A-G

http://identifiers.org/hco/13/GRCh38#67367975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94280862-C-A

67367996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94280883-A-G

http://identifiers.org/hco/13/GRCh38#67369210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94286469-C-A

67369326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94286570-T-A

67369559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94286802-G-A

67369927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94287998-A-G

67370447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94288476-C-T

67371741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94307431-C-T

67371765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94307458-A-G

67371792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94307485-C-T

67371919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94307594-A-T

67372002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94307671-G-A

67372141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94307798-G-C

67372141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94307798-G-T

67372271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94307922-C-G

67372316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94307962-G-A

67372316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94307962-G-C

67372323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94307969-G-A

67372323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94307969-G-T

67372330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94307976-A-G

67372340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94307986-A-G

http://identifiers.org/hco/13/GRCh38#67372361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94308015-C-A

http://identifiers.org/hco/13/GRCh38#67372587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94308233-C-A

67372618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94308264-G-A

67372623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94308269-A-G

67372637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94308282-T-C

67372717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94308408-A-G

67372854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94308553-G-T

67373109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94308787-T-A

67373129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94308807-G-T

67373280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94309078-T-C

67373365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94309163-C-T

67373386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94309184-T-C

67373437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94309230-G-A

67373596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94309374-A-T

67373826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94309594-T-C

67373857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94309622-G-A

67373963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94309718-A-G

67373963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94309718-A-T

67374256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94310032-A-G

67374374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94310152-C-T

67374442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94310222-T-C

67374495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94310275-T-C

67374495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94310275-T-G

67375093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94310857-C-T

http://identifiers.org/hco/13/GRCh38#67375094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#94310858-C-A

67375158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94310924-T-C

67375423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94311283-G-C

67375897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94311865-G-A

67375897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94311865-G-C

67376010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94311984-T-C

67376031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94312005-T-C

67376247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94312553-T-C

67376382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94312662-G-A

67376563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94312790-C-T

67376616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94312836-G-A

67376811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94313029-T-C

67376864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94313086-T-C

67377099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94313318-C-T

67378071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94317217-C-T

67378078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42686
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94317224-A-T