165747844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: 65913592-G-A

165747844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: 65913592-G-T

165747932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: 65913672-G-A

165747993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: 65913728-G-A

165748037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: 65913772-C-T

http://identifiers.org/hco/2/GRCh38#165748092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65913835-C-A

http://identifiers.org/hco/2/GRCh38#165748117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65913860-C-A

165748311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: 65914047-C-T

http://identifiers.org/hco/2/GRCh38#165748335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65914072-C-A

165748335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: 65914072-C-T

http://identifiers.org/hco/2/GRCh38#165748347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65914086-C-A

165748483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: 65914215-G-C

165748483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: 65914215-G-T

http://identifiers.org/hco/2/GRCh38#165748528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65914255-C-A

165748528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: 65914255-C-G

165748630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: 65914354-T-C

http://identifiers.org/hco/2/GRCh38#165748638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65914362-C-A

165748638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: 65914362-C-T

165748668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: 65914399-G-C

165748668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3 prime UTR variant
orthologous variants: 65914399-G-T

http://identifiers.org/hco/2/GRCh38#165748784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65914517-A-C

165748784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: synonymous variant
orthologous variants: 65914517-A-G

165748894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: synonymous variant
orthologous variants: 65914627-G-A

165748963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65914701-T-C

http://identifiers.org/hco/2/GRCh38#165748971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65914709-A-C

165748971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65914709-A-G

165749072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65914837-G-A

165749184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65914951-A-G

165749412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65915160-C-G

165749414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65915162-C-G

http://identifiers.org/hco/2/GRCh38#165749614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65915471-A-C

http://identifiers.org/hco/2/GRCh38#165749616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65915473-A-C

165749616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65915473-A-G

165749628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65915485-G-A

165749628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65915485-G-T

165749721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65915554-G-A

165749721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65915554-G-T

165749919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65915758-T-C

http://identifiers.org/hco/2/GRCh38#165749941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65915780-C-A

165750171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65916007-A-G

165750266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65916093-G-A

http://identifiers.org/hco/2/GRCh38#165750304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65916131-C-A

165750384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65916230-T-C

165750589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65916417-A-G

165751100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65916891-T-A

165751100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65916891-T-C

165751175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65916987-T-C

http://identifiers.org/hco/2/GRCh38#165751328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65917117-C-A

165751539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65917393-A-T

165751831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65917690-A-G

http://identifiers.org/hco/2/GRCh38#165752176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65919133-C-A

165752176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65919133-C-T

165752303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65919221-G-T

165752327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65919242-C-T

165752474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65919384-C-T

165752676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65919550-T-C

165752944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65919832-A-G

165752950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65919838-A-G

165753155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65920093-A-G

165753278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65920207-T-C

165753359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65920268-T-C

165753372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65920281-C-G

165753748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65920647-T-A

165753909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65920865-C-T

165754254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65920991-A-G

165754254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65920991-A-T

165754404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65921016-T-C

http://identifiers.org/hco/2/GRCh38#165754444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65921053-C-A

165754444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65921053-C-T

http://identifiers.org/hco/2/GRCh38#165754480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65921090-A-C

165754480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65921090-A-G

165754480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65921090-A-T

165754495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65921107-A-T

http://identifiers.org/hco/2/GRCh38#165754574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65921186-C-A

165754574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65921186-C-T

165754733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 65921345-A-G

165754769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65921377-A-G

165754769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65921377-A-T

165754804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65921412-T-A

http://identifiers.org/hco/2/GRCh38#165754838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65921440-C-A

165754905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65921478-T-C

http://identifiers.org/hco/2/GRCh38#165754921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65921495-A-C

165755004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: synonymous variant
orthologous variants: 65921578-A-G

165755076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65921650-G-A

165755076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65921650-G-T

165755087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65921665-G-T

165755109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65921685-T-C

http://identifiers.org/hco/2/GRCh38#165755131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65921702-C-A

http://identifiers.org/hco/2/GRCh38#165755477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65921947-C-A

http://identifiers.org/hco/2/GRCh38#165755686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65922124-C-A

165755686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65922124-C-T

165755725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65922160-T-C

165755756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65922190-T-C

165756037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65922437-C-G

165756103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65922479-T-C

165756265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65922598-A-G

165756403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65922925-A-T

165756496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65923079-G-T

165756639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65923217-A-T

165756920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65923595-G-T

165756973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65923801-G-T

165756975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65923803-T-A

165756979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65923807-T-G

165757008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65923835-T-C

http://identifiers.org/hco/2/GRCh38#165757031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65923859-C-A

165757031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65923859-C-T

165757357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65924182-A-G

165757404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65924225-T-G

http://identifiers.org/hco/2/GRCh38#165757440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65924262-C-A

165757577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65924398-C-T

165757682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65924511-T-C

165757716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65924545-C-T

http://identifiers.org/hco/2/GRCh38#165757809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65924642-C-A

165758025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65924808-T-C

165758237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65925013-A-T

http://identifiers.org/hco/2/GRCh38#165758609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65925403-C-A

165758684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65925482-G-A

165758684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65925482-G-T

165758798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 65925596-A-T

165758912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65925708-T-C

165759093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65925885-C-T

http://identifiers.org/hco/2/GRCh38#165759169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65925967-A-C

165759212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65925996-T-C

165759226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926005-G-A

165759226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926005-G-T

http://identifiers.org/hco/2/GRCh38#165759252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65926038-C-A

165759252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926038-C-T

165759253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926039-A-G

http://identifiers.org/hco/2/GRCh38#165759278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65926071-A-C

165759278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926071-A-G

165759278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926071-A-T

165759299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926089-G-C

165759299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926089-G-T

165759319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926117-G-C

165759319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926117-G-T

http://identifiers.org/hco/2/GRCh38#165759389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65926187-C-A

165759389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65926187-C-T

http://identifiers.org/hco/2/GRCh38#165759443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#65926241-A-C

165759443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65926241-A-G

165759478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65926276-G-A

165759478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65926276-G-C

165759488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65926286-T-A

165759542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65926340-A-G

165759542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65926340-A-T

165759596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926395-T-C

165759602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926401-A-T

165760120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926861-T-C

165760161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926889-C-T

165760216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926948-C-G

165760217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65926949-A-G

165760282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65927017-G-A

165760781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65927407-G-C

165760874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65927501-A-T

165761639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65927849-A-G

165761639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65927849-A-T

http://identifiers.org/hco/2/GRCh38#165761742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65927920-A-C

http://identifiers.org/hco/2/GRCh38#165761966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65928118-A-C

165761966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65928118-A-G

165762095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65928253-A-G

165762095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65928253-A-T

165762288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65928456-A-G

165762512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65928674-G-A

165762638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65928812-C-T

165762676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65928861-G-C

165762966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65929041-T-C

165763134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65929164-T-C

165763248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65929263-A-G

165763443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65929443-C-G

165763559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65929519-C-T

165763579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65929538-C-T

165764179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932041-G-A

165764255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932199-C-T

165764261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932205-G-A

165764365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932296-A-G

165764579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932501-T-C

165764596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932518-C-T

165764656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932577-C-T

http://identifiers.org/hco/2/GRCh38#165764754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65932674-C-A

165764754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932674-C-T

165764780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932694-T-G

165764786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932699-C-T

http://identifiers.org/hco/2/GRCh38#165764813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65932726-C-A

165764813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932726-C-T

165764823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932737-T-C

165764823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932737-T-G

165764830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932744-T-C

165764844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932758-T-A

165764844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 65932758-T-C

165764900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 65932805-A-G

165764936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 65932841-T-G

http://identifiers.org/hco/2/GRCh38#165765090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65932996-C-A

165765090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65932996-C-T

165765169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65933092-T-C

165765482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65933367-T-C

165765900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65933490-C-T

165766281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65933865-A-G

http://identifiers.org/hco/2/GRCh38#165766402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65933986-A-C

165766452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65934042-G-A

165766490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65934073-T-C

165766510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65934093-C-G

165766568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65934135-G-A

165766688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65934364-G-A

165766791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65934446-C-G

165766791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65934446-C-T

165767593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65935192-T-C

165767704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65935305-T-C

165767932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65935478-G-A

165768486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65935800-G-A

165768516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65935824-T-A

165768516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65935824-T-C

165768547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65935858-G-A

http://identifiers.org/hco/2/GRCh38#165768571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65935882-A-C

165768649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65935958-T-C

165768660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65935969-C-T

165768708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65936032-A-G

165769747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65936788-T-C

165770049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65937087-A-G

http://identifiers.org/hco/2/GRCh38#165770066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65937098-C-A

165770388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: missense variant
orthologous variants: 65937396-C-T

http://identifiers.org/hco/2/GRCh38#165770423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65937431-C-A

165770423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: missense variant
orthologous variants: 65937431-C-T

165770482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: synonymous variant
orthologous variants: 65937490-A-T

165770535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: missense variant
orthologous variants: 65937543-T-A

165770535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: missense variant
orthologous variants: 65937543-T-C

165770689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: synonymous variant
orthologous variants: 65937697-T-A

165770790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5 prime UTR variant
orthologous variants: 65937797-G-A

http://identifiers.org/hco/2/GRCh38#165770841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65937855-C-A

165770841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65937855-C-T

165770862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65937876-G-A

165770862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65937876-G-T

http://identifiers.org/hco/2/GRCh38#165770885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65937899-C-A

165770958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65937969-A-G

165770995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65938002-A-T

165771316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65938353-T-C

165771375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65938392-A-G

165771405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65938422-G-A

165771405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65938422-G-T

http://identifiers.org/hco/2/GRCh38#165771428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65938444-C-A

165771428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65938444-C-G

http://identifiers.org/hco/2/GRCh38#165771513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65938527-C-A

http://identifiers.org/hco/2/GRCh38#165771576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65938581-C-A

165771576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65938581-C-T

165772162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65942793-G-C

165772194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65942824-T-C

165778682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65943425-A-G

165778736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65943479-G-A

165779159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65943852-C-T

165779203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65943880-G-A

165779213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65943890-C-G

165779304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65943979-T-C

165782721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65944905-T-G

165782804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65944986-G-C

165783009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65945122-T-G

165783381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65945365-C-T

165783393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65945377-C-T

http://identifiers.org/hco/2/GRCh38#165783553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65945504-C-A

165783553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65945504-C-T

165783637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65945632-G-T

165783753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65945806-C-T

165783844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65945888-T-C

165784307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65946311-G-T

165784318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65946322-G-A

165787094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65948008-C-T

165787427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65948321-C-G

165787428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65948322-C-G

165787775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65948656-C-T

165787850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65948730-A-G

165789809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65950410-T-A

http://identifiers.org/hco/2/GRCh38#165789831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65950434-C-A

165790559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65951086-A-G

165790683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65951171-A-T

165790728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65951218-A-T

165791440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65952346-A-T

165791844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65952781-T-A

165791844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65952781-T-C

http://identifiers.org/hco/2/GRCh38#165791852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65952789-C-A

165792117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65953042-T-G

165792606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65953562-G-A

165792672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65953635-T-C

165792699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65953665-T-C

165793016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65953981-G-A

165793553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65954502-G-A

165793649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron_variant, missense_variant
orthologous variants: 65954589-C-T

165793764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65954686-G-A

165793764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65954686-G-T

http://identifiers.org/hco/2/GRCh38#165793846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65954737-C-A

165793903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65954786-G-A

165793903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65954786-G-C

165793903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron variant
orthologous variants: 65954786-G-T

165794048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65954900-G-T

165794059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 65954911-A-G

165794059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 65954911-A-T

http://identifiers.org/hco/2/GRCh38#165794075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65954930-C-A

165794075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65954930-C-G

165794075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 65954930-C-T

165794114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 65954969-T-C

165794229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65955084-G-C

165794229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65955084-G-T

165794301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: intron_variant, missense_variant
orthologous variants: 65955155-C-T

165794367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65955210-G-A

165794367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65955210-G-C

165794367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65955210-G-T

http://identifiers.org/hco/2/GRCh38#165794567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65955375-C-A

http://identifiers.org/hco/2/GRCh38#165794579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4125
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#65955385-C-A