175796314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5 prime UTR variant
orthologous variants: 54456409-T-C

175796369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5 prime UTR variant
orthologous variants: 54456443-G-A

175796369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5 prime UTR variant
orthologous variants: 54456443-G-T

175796562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5 prime UTR variant
orthologous variants: 54456649-G-C

175796562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5 prime UTR variant
orthologous variants: 54456649-G-T

http://identifiers.org/hco/5/GRCh38#175796597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54456683-C-A

175796597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5 prime UTR variant
orthologous variants: 54456683-C-T

175796808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54456889-C-G

175796892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54456955-G-A

175797119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54457109-C-T

175800271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54460268-G-A

175800356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54460353-A-G

175800539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54460425-T-C

175800586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54460454-G-A

http://identifiers.org/hco/5/GRCh38#175800755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54460589-C-A

175800755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54460589-C-G

175800755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54460589-C-T

175800888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54460710-G-A

175801120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54460950-T-A

175801793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54462747-C-T

175802591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54463527-G-A

175802635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54463570-G-C

175802780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54463733-G-A

http://identifiers.org/hco/5/GRCh38#175805686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54464079-A-C

175805686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54464079-A-G

175805711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54464104-G-A

175805711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54464104-G-T

175805736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54464132-G-A

175805736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54464132-G-T

175806124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54464427-C-T

175806152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54464446-C-G

175806263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54464535-A-T

175806270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54464542-G-A

175808012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54465147-T-G

175808111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54465253-C-T

175808544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54465643-A-T

175808922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54465979-C-T

175809029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54466085-A-T

175809128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54466171-G-A

175809128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54466171-G-T

175809143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54466194-G-T

http://identifiers.org/hco/5/GRCh38#175809155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54466206-C-A

175809155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54466206-C-T

http://identifiers.org/hco/5/GRCh38#175809210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54466246-C-A

175809283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54466282-C-T

175809398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54466388-T-C

175809431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54466423-C-T

175809471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54466463-A-G

175809486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54466478-A-G

http://identifiers.org/hco/5/GRCh38#175809495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54466487-C-A

175809495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54466487-C-G

175809495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54466487-C-T

175809614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54466581-C-T

175809691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54466678-C-T

175809708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54466695-C-T

175810110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54467090-C-T

175810152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54467131-G-T

http://identifiers.org/hco/5/GRCh38#175810213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54467174-C-A

175810230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54467191-T-A

175810291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54467258-G-A

175810363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54467328-C-T

175810636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54467558-A-G

175810636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54467558-A-T

175810796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54467716-C-T

175810798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54467718-C-T

175811175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54468098-G-A

175812203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54468980-C-T

http://identifiers.org/hco/5/GRCh38#175812232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54468951-A-C

175812232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54468951-A-G

http://identifiers.org/hco/5/GRCh38#175812677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54469652-C-A

175812677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54469652-C-T

http://identifiers.org/hco/5/GRCh38#175812863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54469830-C-A

175813082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54470030-G-A

175813082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54470030-G-T

175813139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54470083-G-A

175813624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54470675-G-T

175813704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54470819-G-A

175813704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54470819-G-C

175813761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54470913-G-A

175813799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54471029-G-A

175813959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54471271-G-A

175814036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54471374-C-T

175814181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54471516-C-T

175814262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54471592-C-T

175814494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54471777-C-T

175814502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54471789-G-T

175814569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54471856-C-T

http://identifiers.org/hco/5/GRCh38#175814753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54472033-C-A

175814753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54472033-C-T

175814903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54472147-G-A

175814903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54472147-G-T

175814944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54472185-G-A

175814974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54472196-G-T

175815002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54472218-G-A

175815143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54472358-C-T

175815163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54472379-C-G

175815192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54472412-G-A

175815192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54472412-G-C

175815253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54472454-G-A

175815253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54472454-G-C

175815560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54472669-G-T

175815892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54472973-C-T

175816044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54473100-T-C

175816044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54473100-T-G

175816120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54473166-G-A

175816128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54473174-C-T

175816564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54473304-G-A

175816564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54473304-G-C

175817635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54473751-G-T

175817744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54473851-G-A

175817761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54473868-G-A

175817830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54473945-T-A

175818089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54474287-G-C

http://identifiers.org/hco/5/GRCh38#175818418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54474554-C-A

175818486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54474623-T-G

175819778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54475714-G-A

175820130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54476014-G-A

175820130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54476014-G-C

175820379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54476465-G-C

175820481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54476569-C-T

175820577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54476677-A-G

175820791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54476868-G-A

175820795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54476872-T-C

175820878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54476953-T-G

175820910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54476986-G-A

http://identifiers.org/hco/5/GRCh38#175821111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54477285-C-A

175821111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54477285-C-T

175821117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54477291-G-A

175821491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54477534-T-A

http://identifiers.org/hco/5/GRCh38#175821781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54477630-A-C

175821824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54477674-A-T

175821972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54477815-G-A

175822122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54477981-T-C

175822468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54478286-T-A

175822588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54478404-A-G

175823189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54479064-T-C

175823275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54479149-G-A

175823470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54479317-G-A

175823470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54479317-G-T

http://identifiers.org/hco/5/GRCh38#175823471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54479318-A-C

175823489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54479337-G-A

175823711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54479858-T-C

175823849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54479989-C-T

175823948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54480084-C-T

175824074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54480210-T-C

175824379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54480501-G-C

175824417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54480550-G-T

175827925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54482645-C-T

175828184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54483070-T-A

175828261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54483142-C-T

175828315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54483193-G-A

175828429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54483309-A-G

175828429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54483309-A-T

175828534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54483399-G-A

175828561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54483425-G-A

175828717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54483572-G-A

175828972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54483760-G-A

175828975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54483763-C-T

175829025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54483812-A-T

175829151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54483902-T-C

175829366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54484074-G-A

175829583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54484285-A-G

175829796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54484970-C-G

175829796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54484970-C-T

175830058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54485190-G-A

175830164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54485297-T-C

175830172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54485343-G-C

http://identifiers.org/hco/5/GRCh38#175830183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54485354-A-C

175830244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54485435-G-T

175830278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54485468-A-G

175830397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54485549-G-A

http://identifiers.org/hco/5/GRCh38#175830453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54485590-A-C

175830469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54485606-C-T

175830485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54485617-T-G

175830671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54485804-C-G

175831060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54486172-C-G

175831079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54486189-T-C

175831194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54486292-G-C

175831260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54486358-C-G

175831496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54486595-C-T

175831842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54486924-G-T

175831846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54486928-G-A

175831855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54486933-C-T

175831932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54487006-A-G

175831967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54487040-A-G

175832083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54487180-T-G

175832542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54487577-G-A

175832542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54487577-G-C

175832661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54487693-A-G

175832662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54487694-C-T

175832745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54487791-C-T

175832807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54487839-G-A

175832866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54487892-A-G

175833153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54488225-T-A

175833430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54488497-T-C

175833530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54488588-A-G

175833757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54488811-G-A

175833757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54488811-G-T

175834087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54489136-C-T

175834212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54489251-A-G

175834250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54489266-T-C

175835318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54490050-A-T

http://identifiers.org/hco/5/GRCh38#175835407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54490139-C-A

http://identifiers.org/hco/5/GRCh38#175836494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54490589-A-C

175836792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54490888-C-T

175836924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54490982-G-C

175837126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54491164-A-G

175837479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54491465-G-A

175837479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54491465-G-T

175837768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54491688-G-T

175837779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54491699-T-C

175837804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54491724-G-A

175837804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54491724-G-T

http://identifiers.org/hco/5/GRCh38#175837882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54491936-C-A

175837882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54491936-C-G

175837890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54491942-G-A

175837890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54491942-G-T

175837891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54491943-T-C

175837923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54491975-G-T

175838826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54492749-A-G

175838954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54492837-C-G

175838964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54492847-G-A

175839003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54492897-C-G

175839003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54492897-C-T

175840863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54494996-T-G

175840964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54495102-C-T

175840973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54495111-G-A

175841237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54495362-C-T

http://identifiers.org/hco/5/GRCh38#175841348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54495442-C-A

175841444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54495535-C-T

175841586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54495665-C-T

175841589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54495667-C-G

175841813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54495915-C-T

175845512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54496105-G-A

175846131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54496635-C-G

http://identifiers.org/hco/5/GRCh38#175846141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54496642-C-A

175846141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54496642-C-T

175846290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54496776-G-A

175846471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54496919-T-A

175846471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54496919-T-C

http://identifiers.org/hco/5/GRCh38#175846484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54496936-A-C

175846638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54497250-G-A

175846876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54497433-T-C

175847115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54497636-C-T

175847177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54497702-C-G

175847304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54497853-G-A

175847304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54497853-G-T

175847470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54498010-T-C

175847508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54498055-T-C

175847516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54498063-G-A

175847519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54498066-C-T

http://identifiers.org/hco/5/GRCh38#175847601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54498172-A-C

175847601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54498172-A-G

175847823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54498353-C-G

175847927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54498405-A-G

175848339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54498790-G-A

175848529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54498924-G-T

175848646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54499003-A-G

175848756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54499110-T-C

175848814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54499165-G-T

175848906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54499259-T-C

175848919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54499272-G-C

175848919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54499272-G-T

175849113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54499409-G-T

175849153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54499420-G-A

175849420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54499674-G-C

175849531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54499760-C-T

175849897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54500038-G-C

175849904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54500048-T-C

175850089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54500241-C-T

175850364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54500516-C-T

175850367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54500519-G-A

175850367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54500519-G-C

175850815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54500887-C-T

175850826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54500898-G-A

http://identifiers.org/hco/5/GRCh38#175851099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54501112-C-A

175851099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54501112-C-T

175851121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54501134-G-A

175851121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54501134-G-C

175851202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54501187-G-A

175851249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54501233-A-T

175851380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54501373-C-G

175851490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54501463-C-T

175851526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54501559-C-G

175851770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54502056-G-A

175852363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54502611-G-A

175853057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54503033-C-T

175853059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54503035-C-T

175853159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54503140-T-A

175853946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54503403-G-C

175853953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54503410-G-A

175853953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54503410-G-T

175854203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54503630-A-T

175854452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54503806-G-C

175854982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54505498-C-T

175855495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54506241-G-A

175855538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54506280-T-C

175855809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54506562-G-A

175856047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54506729-T-C

175856058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54506735-G-T

175856138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54506784-C-T

175856240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54506866-A-G

175856355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54506976-T-C

http://identifiers.org/hco/5/GRCh38#175856360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54506981-C-A

175856364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54506985-G-A

175856403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54507024-T-A

175856456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54507077-A-G

175856638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54507259-T-C

175856795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54507391-G-A

175858765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54507699-T-G

175858815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54507743-C-T

175858977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54507876-T-A

175859007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54507918-T-C

175859166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54508050-T-C

http://identifiers.org/hco/5/GRCh38#175859175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54508059-A-C

175859337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54508223-G-C

175859448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54508332-G-A

175859489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54508362-G-A

175860722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54508834-G-A

http://identifiers.org/hco/5/GRCh38#175861090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54509150-A-C

175861217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54509275-C-G

175861266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54509323-A-G

175861516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54509551-G-A

175861516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54509551-G-T

175861529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54509564-G-A

175861529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54509564-G-T

175861590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54509624-A-T

175861594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54509628-G-A

175861594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54509628-G-T

175861632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54509665-G-A

http://identifiers.org/hco/5/GRCh38#175861663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54509696-C-A

175861664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54509697-A-G

http://identifiers.org/hco/5/GRCh38#175861832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54509861-C-A

175861873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54509901-G-T

175861889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54509915-T-C

175862064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54510084-G-T

http://identifiers.org/hco/5/GRCh38#175862099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54510100-C-A

175862150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54510149-A-G

175863155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54511434-A-G

175863711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54511948-G-A

175863741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54511980-A-G

175864115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54512362-G-A

175864549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54512788-G-A

175864624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54512843-G-C

175864626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54512845-A-G

175864629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54512848-G-A

http://identifiers.org/hco/5/GRCh38#175864706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54512897-A-C

175864706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54512897-A-G

175865423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54513594-A-G

175865569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54513721-C-T

175865770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54513943-C-G

175865781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54513954-G-A

175865810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54513981-G-A

175865853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54514022-A-T

175866107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54514263-G-A

175866329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54514450-T-C

175866437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54514554-G-A

175866437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54514554-G-C

175866583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54514699-G-A

175866672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54514779-C-G

175866726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54514836-G-A

175867240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54515016-G-A

175867269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54515045-C-T

175867279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54515065-G-A

175867582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54515352-C-G

175867582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54515352-C-T

175867708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54515459-G-A

175867727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54515478-C-G

175867727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54515478-C-T

175867762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54515503-C-G

175867773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54515514-C-T

175867853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54515580-T-C

175867879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54515606-C-G

175868419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54516125-C-T

175868696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54516389-G-A

175868696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54516389-G-T

175868740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54516433-A-G

http://identifiers.org/hco/5/GRCh38#175868767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54516530-C-A

175868774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54516560-G-A

175869155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54516928-C-T

175869269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54517048-G-C

175869294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54517073-G-C

175869528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54517336-C-T

175869700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54517533-A-G

175869806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54517616-G-A

175870526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54518235-T-C

175870596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54518314-G-C

175870887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54518574-C-T

175871137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54518819-T-G

175871236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54518925-T-C

175871261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54518951-C-T

175871361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54519048-G-A

175871440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54519118-A-G

175871528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54519205-G-T

175871615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54519299-G-A

175871615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54519299-G-T

http://identifiers.org/hco/5/GRCh38#175871616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54519300-C-A

175871783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54519457-G-A

175871783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54519457-G-T

175871789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54519463-C-T

175871799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54519472-T-C

http://identifiers.org/hco/5/GRCh38#175871846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54519513-A-C

175871846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54519513-A-T

http://identifiers.org/hco/5/GRCh38#175871933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54519581-C-A

175871933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54519581-C-T

175871950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54519598-G-A

175871950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54519598-G-T

http://identifiers.org/hco/5/GRCh38#175871998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54519636-C-A

http://identifiers.org/hco/5/GRCh38#175872001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54519639-A-C

http://identifiers.org/hco/5/GRCh38#175872027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54519665-C-A

http://identifiers.org/hco/5/GRCh38#175872107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54519747-C-A

http://identifiers.org/hco/5/GRCh38#175872129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54519769-C-A

175872129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54519769-C-T

175872143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54519783-G-A

175872258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54519877-G-A

175872258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54519877-G-C

175872258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54519877-G-T

175872318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54519928-G-A

175872318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54519928-G-T

175872321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54519931-G-A

175872321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54519931-G-T

175872465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54520048-G-A

175872539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54520111-G-A

175872544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54520116-A-G

175872660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54520233-T-C

http://identifiers.org/hco/5/GRCh38#175872662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54520235-C-A

175872716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54520303-G-A

175872716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54520303-G-T

http://identifiers.org/hco/5/GRCh38#175872725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54520310-C-A

175872725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54520310-C-T

175872810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54520410-A-G

175872857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54520451-C-T

175872867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54520460-G-A

175872887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54520480-G-A

175872887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54520480-G-T

175872988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54520586-G-A

175872988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54520586-G-T

http://identifiers.org/hco/5/GRCh38#175873050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#54520644-C-A

175873064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54520655-G-A

175873064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54520655-G-T

http://identifiers.org/hco/5/GRCh38#175873159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54520744-C-A

175873159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54520744-C-T

175873576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54521120-C-T

175873580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54521124-G-C

175873810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54521320-G-A

175873906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54521413-G-C

175873931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54521438-A-T

175874151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54521673-T-G

175874303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54521768-C-T

175874727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54522102-G-C

175875107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54522433-G-A

175875533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54522824-G-C

http://identifiers.org/hco/5/GRCh38#175876936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54524318-C-A

175876966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54524342-G-C

http://identifiers.org/hco/5/GRCh38#175877243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54524577-C-A

175877243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54524577-C-T

175877552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54524886-G-T

175878191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54525732-G-A

175878191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54525732-G-T

175878215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54525756-C-T

175878217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54525758-G-T

175878342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54525874-A-G

175878489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54526245-T-C

http://identifiers.org/hco/5/GRCh38#175878503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54526259-C-A

175878503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54526259-C-G

175878503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54526259-C-T

175878785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54526518-C-G

175878796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54526529-T-A

175878796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron_variant, undefined
orthologous variants: 54526529-T-C

http://identifiers.org/hco/5/GRCh38#175878882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54526598-C-A

175878882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54526598-C-T

175878885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54526601-T-A

175878885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54526601-T-C

175879032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: missense_variant, undefined
orthologous variants: 54526749-C-G

175879205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54526879-C-T

175879319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54526969-T-C

175879523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54527035-A-G

175879610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: intron variant
orthologous variants: 54527118-A-G

175879967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: synonymous variant
orthologous variants: 54527444-G-A

175880197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54527694-T-G

175880209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54527705-C-T

http://identifiers.org/hco/5/GRCh38#175880214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54527710-C-A

http://identifiers.org/hco/5/GRCh38#175880313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54528085-A-C

175880313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54528085-A-G

175880313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54528085-A-T

http://identifiers.org/hco/5/GRCh38#175880413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54528192-C-A

175880413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54528192-C-T

175880477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54528258-T-A

175880477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54528258-T-C

175880516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54528297-T-C

http://identifiers.org/hco/5/GRCh38#175880587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54528372-C-A

http://identifiers.org/hco/5/GRCh38#175880639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54528425-A-C

http://identifiers.org/hco/5/GRCh38#175880880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54528663-A-C

175880880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54528663-A-G

175880880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54528663-A-T

175880976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54528760-G-A

175881110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54528892-A-G

175881110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54528892-A-T

175881269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54529032-G-A

175881269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54529032-G-T

175881344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54529094-G-T

175881380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54529130-T-C

175881399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54529150-A-G

175881403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54529154-G-A

175881451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54529204-A-G

175881518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54529260-T-C

175881609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54529349-G-A

175881609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54529349-G-T

http://identifiers.org/hco/5/GRCh38#175881660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54529410-C-A

175881914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54529662-G-T

http://identifiers.org/hco/5/GRCh38#175882164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54529905-C-A

175882164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54529905-C-T

http://identifiers.org/hco/5/GRCh38#175882430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54530189-C-A

175882430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54530189-C-T

http://identifiers.org/hco/5/GRCh38#175882511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54530271-C-A

175882511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54530271-C-G

175882518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54530278-G-A

175882518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54530278-G-T

175882626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54530376-C-T

175882779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54530503-T-A

175883167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54530914-G-A

175883167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54530914-G-T

175883171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54530918-G-A

175883171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54530918-G-T

175883221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54530969-G-A

175883231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54530979-G-T

175883487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54531192-C-T

175883600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54531308-G-T

175883705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54531410-G-A

175883705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54531410-G-C

175883705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: 54531410-G-T

http://identifiers.org/hco/5/GRCh38#175883709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54531414-C-A

http://identifiers.org/hco/5/GRCh38#175883995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#54531704-C-A