158963036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: non coding transcript exon variant
orthologous variants: 67679232-T-A

158963167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: non coding transcript exon variant
orthologous variants: 67679304-T-C

158963307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67679368-G-T

158963331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67679389-G-C

158963331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67679389-G-T

158963369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67679432-A-G

158963709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67680596-A-G

http://identifiers.org/hco/3/GRCh38#158963730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67680617-A-C

158963909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67680797-T-G

158963997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67680887-A-G

158964110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67680996-T-A

158964144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67681027-A-G

158965237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67681504-T-C

158965703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67681951-T-C

158965763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67681984-G-A

158969735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67686791-G-A

158969878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67686960-T-G

158970469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67687539-G-T

158970703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67687909-G-A

158970736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67687941-A-G

158970772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67687978-A-G

158970780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67687986-G-A

158970924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67688141-T-C

158970943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67688161-A-T

158971002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67688217-C-T

158973276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67690234-T-C

158973348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67690274-A-T

158973411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67690346-G-T

158973573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67690497-A-G

158973790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67690728-G-A

158973806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67690743-C-T

158973817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67690754-A-G

158973835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67690772-C-G

158973842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67690782-C-G

158973904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67690849-A-G

158973967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67690909-T-A

158974056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67690998-T-C

158974412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67691629-T-C

158974578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67691799-G-T

158974733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67692335-A-G

158974743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67692345-A-G

158974874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67692505-A-T

158974978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67692599-T-G

158974986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67692607-A-G

158975035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67692659-G-A

158975116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67692735-A-G

158975157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67692775-C-G

158975182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67692793-A-G

158975214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67692820-A-G

158975315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67692920-A-G

158975551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67693163-T-C

158975551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67693163-T-G

158975603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67693215-G-A

158975849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67693460-T-C

158975850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67693461-G-A

158976242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67693834-T-A

158976404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67693981-T-A

158976502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67700963-G-A

158976521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67700986-C-T

158976550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67701015-C-T

158976605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67701054-C-G

158976897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67708142-T-C

158977084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67708297-A-G

158977154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67708328-C-T

158977466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67708459-G-A

158977488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67708479-A-G

158977549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67708540-C-T

158977807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67708796-A-T

158977923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67708911-G-A

158978058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67709032-T-C

158978113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67709091-G-T

158978198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67709171-T-G

158978486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67709460-T-C

158978730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67709931-C-T

158978827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710026-G-A

158978827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710026-G-T

158978868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710066-C-G

158979124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710294-G-A

158979145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710315-G-A

158979161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710331-T-C

158979169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710339-G-A

158979306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710467-T-C

158979309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710470-G-C

158979387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710555-G-A

158979417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710584-T-G

158979565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710758-T-G

158979567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710760-G-A

158979585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710778-G-T

http://identifiers.org/hco/3/GRCh38#158979596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67710788-C-A

158979641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710833-A-G

158979649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67710841-G-T

158980430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67711137-C-T

158980522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67711203-A-G

158980522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67711203-A-T

158980557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67711227-G-C

158980786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67711663-G-C

158980851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67711728-T-C

158980988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67711871-C-T

158981126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67712017-G-A

158981142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67712033-G-A

http://identifiers.org/hco/3/GRCh38#158981145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67712036-C-A

158981603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67712065-T-A

158981608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67712070-A-G

158981633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67712095-T-A

158981751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67712211-C-T

158981859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67712330-G-A

158981859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67712330-G-T

158981860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67712331-T-G

158981928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67712398-C-T

http://identifiers.org/hco/3/GRCh38#158981992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67712432-C-A

158982048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67712486-A-G

158982433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67712896-C-G

158982609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67713070-C-T

158982680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67713141-T-C

http://identifiers.org/hco/3/GRCh38#158982842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67713296-C-A

158982924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67713459-C-T

158982965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67713527-G-A

158982981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67713567-A-G

158983236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67713967-T-C

158983426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67714161-C-T

158983524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67714259-T-G

158983608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67714343-G-A

158983900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67714631-C-T

158984004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67714907-C-T

158984045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67714945-G-A

158984142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67715076-A-T

158984502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67715343-A-G

158984522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67715355-T-C

158984838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67715885-T-G

158984972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67715986-C-T

158985472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67717445-G-A

158992084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67717593-C-G

158992086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67717595-G-A

158992243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67717742-G-T

158992268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67717777-T-C

158992574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67718051-G-A

158992574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67718051-G-C

158992798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67718273-G-A

158993389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67718897-T-A

http://identifiers.org/hco/3/GRCh38#158993422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67718931-C-A

158993422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67718931-C-T

158993517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67719023-G-A

http://identifiers.org/hco/3/GRCh38#158993537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67719043-C-A

158993827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67719336-G-A

158993875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67719384-G-A

158994426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67719931-C-T

158994537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67720046-C-T

158994671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67720181-G-A

158994671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67720181-G-T

158994876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67720383-T-C

158994922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67720429-A-G

158994933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67720444-A-G

158994988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67720512-G-A

158994988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67720512-G-C

158995020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67720542-A-G

158995078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67720599-A-T

158995250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67721535-A-G

158995439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67721849-C-G

158995637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67722572-G-C

158995645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67722580-G-A

158995661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67722596-G-T

158995681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67722616-A-G

158995919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67722866-T-C

158995975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67722933-A-G

158995983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67722976-T-C

158995984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67722977-C-T

158995992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67722992-A-G

158996079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723077-G-A

158996079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723077-G-C

158996079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723077-G-T

http://identifiers.org/hco/3/GRCh38#158996100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67723093-A-C

158996100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723093-A-T

158996107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723097-T-A

158996118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723103-A-G

158996524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723557-T-C

158996544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723577-G-A

158996550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723583-G-C

158996564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723597-G-A

158996593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723626-G-A

158996593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723626-G-T

158996660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723691-A-G

158996720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723730-G-A

158996720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723730-G-C

158996756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723765-C-T

158996968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723973-A-G

158996986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67723991-A-T

158997096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67724068-T-C

158997158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67724126-A-G

158997222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67724182-T-A

http://identifiers.org/hco/3/GRCh38#158997226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67724188-A-C

158997245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67724199-T-C

158997335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67724289-T-C

158997394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67724330-G-C

158997432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67724368-G-T

http://identifiers.org/hco/3/GRCh38#158997487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67724427-A-C

158997487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67724427-A-T

158997616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67724552-A-G

158997685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67724623-T-C

158997695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67724632-C-T

http://identifiers.org/hco/3/GRCh38#158998003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67724920-C-A

158998061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67724978-G-A

158998061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67724978-G-T

158998236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67725162-A-G

http://identifiers.org/hco/3/GRCh38#158998439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67725432-C-A

158998439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67725432-C-G

158998455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67725459-C-T

158998497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67725526-T-A

158998683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67725736-G-T

http://identifiers.org/hco/3/GRCh38#158998703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67725756-C-A

158998851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67725893-T-G

158999688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67731489-A-G

159000181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67733028-T-G

159000373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67733189-A-G

http://identifiers.org/hco/3/GRCh38#159000401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67733218-C-A

159000461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67733277-T-C

159000509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67733325-A-G

159000509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67733325-A-T

159000981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67733476-T-C

159001004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67733499-T-C

159001107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67733602-A-G

159001107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67733602-A-T

159001598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67734082-G-A

159001670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67734119-G-A

159001752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67734192-T-A

159001800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67734243-A-G

159001828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67734270-C-T

159001881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67734301-A-G

159001938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67734356-C-T

159002416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67734784-A-T

159002481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67734847-A-T

159002613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67734977-T-A

159002851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67735215-G-A

159002980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67735337-G-T

159003014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67735371-T-C

159003015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67735372-C-T

159003043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67735425-G-T

159003074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67735449-G-A

159003145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67735515-A-G

159003155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67735528-C-T

159003304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67735660-T-G

159003379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67735734-G-A

159003420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67735778-T-C

159003679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67736030-G-T

159003738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67736081-C-T

159003749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67736092-C-T

159003757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67736117-T-C

159003852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67736213-T-A

159003852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67736213-T-G

159003990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67736344-A-T

159004072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67736436-G-A

159004202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67736564-A-G

159004258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67736615-G-A

159004309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67736664-A-G

159004501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67736815-C-G

159004695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67737337-G-T

159004859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67737591-T-C

159004874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67737606-G-A

http://identifiers.org/hco/3/GRCh38#159005167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67737856-C-A

159005565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67738249-G-A

159005620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67738295-A-G

159006799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67738771-T-C

159006799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67738771-T-G

159006923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67738890-G-A

159006923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67738890-G-C

159006927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67738894-A-G

159006976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67738941-T-A

159007016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67738980-G-A

159007016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67738980-G-T

159007190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67739100-T-G

159007680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67739744-A-G

159008020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67740291-G-T

159008072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67740346-A-G

159008754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67740938-T-C

159008834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67741021-T-C

159010012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67741173-G-A

159010070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67741228-G-A

159010118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67741276-G-C

http://identifiers.org/hco/3/GRCh38#159010239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67741397-C-A

159010239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67741397-C-G

159010255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67741413-G-A

159010304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67741466-A-T

159010611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67741771-T-G

159012197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67742020-A-G

159012264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67742086-G-C

http://identifiers.org/hco/3/GRCh38#159012365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67742186-C-A

159012369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67742190-T-C

159012378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67742203-T-G

159012604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67743657-C-T

159012613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67743668-T-C

159012657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67743714-G-A

159012710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67743767-T-C

159012910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67743966-A-T

159012914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67743974-A-T

159013118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67744214-T-C

159013165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67744264-G-C

159013182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67744281-A-T

159013210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67744309-A-G

159013787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67746064-G-A

159014029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67746273-G-A

159014029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67746273-G-C

159014140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67746387-A-G

159014163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67746412-T-C

159014170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67746419-T-A

159014227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67746475-A-G

http://identifiers.org/hco/3/GRCh38#159014262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67746522-A-C

159014426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67746668-C-T

159014451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67746693-G-A

159014523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67746755-A-T

http://identifiers.org/hco/3/GRCh38#159014614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67746830-A-C

159014677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67746865-T-C

159014745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67746934-G-A

159014785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67746974-C-T

159014911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747095-C-T

159014963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747146-G-A

159014985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747168-C-T

159015008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747191-G-A

159015050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747243-A-G

159015197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747382-G-A

159015229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747415-C-G

159015292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747472-A-G

159015689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747561-A-G

http://identifiers.org/hco/3/GRCh38#159015733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67747610-A-C

159015896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747770-G-T

159015967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747847-T-G

159016081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747930-T-C

159016108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747957-G-A

159016218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67748053-C-T

159016234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67748075-G-A

159016234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67748075-G-C

159016265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67748106-G-C

159016370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67748964-G-A

159016610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67749162-C-T

159016799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67749332-T-G

159016931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67749430-G-A

159017006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67749500-T-G

159017680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67750342-C-T

159017685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67750347-G-T

159017878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67750488-T-C

159018008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67750574-G-A

159018385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67750878-T-A

http://identifiers.org/hco/3/GRCh38#159018400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67750893-C-A

159018580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67751051-G-T

159018757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67751214-G-A

159018983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67751725-G-C

159019025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67751766-A-G

159019132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67751869-A-G

159028295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67752367-A-G

159028420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67752509-T-A

159028584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67752676-A-G

159028910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67752994-A-G

159028964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67753042-G-A

159029016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67753092-T-C

159029258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756049-C-T

159029304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756096-G-A

159029349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756145-A-G

159029363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756156-G-A

159029415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756207-C-G

159029415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756207-C-T

159029459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756246-A-G

159029529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756319-C-T

159029552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756342-A-G

http://identifiers.org/hco/3/GRCh38#159029616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67756399-A-C

159029616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756399-A-G

159030523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756794-T-G

159030729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756981-C-T

159031092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67757309-T-C

159031215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67757599-A-G

159031262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67757702-T-C

159031308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67757748-A-G

159031382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67757821-A-T

159036579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67762477-A-G

159036842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67762728-G-C

http://identifiers.org/hco/3/GRCh38#159036893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67762791-A-C

http://identifiers.org/hco/3/GRCh38#159037385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67763259-A-C

159037558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67763392-A-T

159037639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67763470-G-C

http://identifiers.org/hco/3/GRCh38#159037688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67763527-C-A

159037800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67763673-G-T

159037882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67763887-A-G

159037901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67763906-T-C

http://identifiers.org/hco/3/GRCh38#159038598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67764713-C-A

159038666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67764771-G-C

159038815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67764899-G-T

159038839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67764923-G-T

159039028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67765006-T-A

http://identifiers.org/hco/3/GRCh38#159039061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67765022-A-C

159039236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67765122-C-G

159039236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67765122-C-T

159039273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67765161-A-G

159039274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67765162-T-C

159040752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67767000-C-T

159041064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67767829-C-G

159041281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67768046-G-A

159041367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67768136-G-A

159041396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67768165-A-G

159041445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67768215-T-C

159041651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67768416-G-T

159042275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67769137-G-C

159042396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67769257-G-T

159042649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772664-G-A

159042649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772664-G-T

159042790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772808-A-G

159042795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772813-T-C

http://identifiers.org/hco/3/GRCh38#159042871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67772881-C-A

159042885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772886-A-T

159043085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67773012-G-A

159043230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67773112-G-T

159043397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67773260-T-G

159043451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67773318-T-A

159043498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67773365-A-G

159043566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67773439-T-G

159044617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67784356-C-T

159044651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67784390-A-G

159044711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67784449-G-A

159045160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67774613-G-T

159045188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67774643-C-T

159045195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67774650-T-C

159045348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67774779-A-G

159045549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67774982-T-C

159045621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67775050-G-A

159045794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67775218-G-C

http://identifiers.org/hco/3/GRCh38#159045817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67775240-C-A

159045817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67775240-C-T

159045819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67775242-G-A

159045947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67775369-G-A

159046000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67775415-C-T

159046002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67775417-G-A

159046004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67775419-T-A

159046004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67775419-T-C

http://identifiers.org/hco/3/GRCh38#159046634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67776024-C-A

159046886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67776279-G-C

159046942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67776333-C-T

159047119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67776514-A-G

159047160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67776555-C-T

159047399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67776802-A-T

159047955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67777629-G-T

159048383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778079-A-G

http://identifiers.org/hco/3/GRCh38#159048989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67778874-A-C

159048989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778874-A-G

http://identifiers.org/hco/3/GRCh38#159049019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67778891-C-A

http://identifiers.org/hco/3/GRCh38#159053316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67783117-C-A

159053686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67783459-T-G

http://identifiers.org/hco/3/GRCh38#159054123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67783871-A-C

159054164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67783898-C-G

http://identifiers.org/hco/3/GRCh38#159054475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67784151-C-A

159054770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67784448-C-T

159054835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67784516-C-T

159054947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67784608-T-G

159055434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67784802-T-C

159055623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67785008-A-G

159055658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67785041-G-A

159055752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67785133-G-A

159055797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67785175-C-T

http://identifiers.org/hco/3/GRCh38#159055869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67785253-C-A

159055869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67785253-C-G

159057167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67785658-C-G

159057196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67785685-A-G

159057251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67785740-C-T

159057411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67785887-C-T

159057433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67785912-G-A

159057483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67785962-A-G

159057651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67786115-G-A

159057782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67786249-G-T

159057873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67786382-T-C

159057996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67786501-A-G

159058126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67786644-T-G

159058160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67786678-G-C

159058309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67786832-G-A

http://identifiers.org/hco/3/GRCh38#159058467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67787048-A-C

159058467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67787048-A-G

159058714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67787474-G-C

159059058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67787769-C-T

http://identifiers.org/hco/3/GRCh38#159059085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67787798-A-C

159059359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67787994-T-G

http://identifiers.org/hco/3/GRCh38#159059433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67788030-A-C

159059503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67788100-A-G

159061023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67790400-G-C

http://identifiers.org/hco/3/GRCh38#159061052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67790430-C-A

159061158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67790525-A-T

http://identifiers.org/hco/3/GRCh38#159061188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67790555-A-C

159061188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67790555-A-G

159061225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67790637-A-G

159061225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67790637-A-T

159061294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67790724-A-T

159061329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67790758-G-A

159062056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791729-C-T

159062119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791785-A-G

159062191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791835-C-G

159062191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791835-C-T

159062192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791836-G-A

159062222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791866-A-G

159062246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791890-G-A

159062300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791946-G-T

159062314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791963-T-A

159062370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792021-A-G

159062440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792091-C-T

http://identifiers.org/hco/3/GRCh38#159062441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67792092-A-C

159062441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792092-A-G

159062458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792109-T-C

159062460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792111-C-T

159062551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792223-T-G

159062851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792523-G-A

http://identifiers.org/hco/3/GRCh38#159062960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67792634-C-A

159062960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792634-C-T

http://identifiers.org/hco/3/GRCh38#159062981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67792653-C-A

159062981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792653-C-T

159063042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792714-A-G

159063134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792806-G-T

159063227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792886-G-A

159063227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792886-G-C

http://identifiers.org/hco/3/GRCh38#159063303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67792959-C-A

159063304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792960-C-T

159063384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67793018-A-G

159063456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67793090-C-T

159063474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67793113-T-C

159063653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67793362-T-C

159063794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67793482-G-A

159063794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67793482-G-C

159063794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67793482-G-T

159063838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67793513-C-T

159064070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67793745-A-G

159064355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67794019-G-A

159064743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67794404-A-G

159064761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67794425-A-G

159064791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67794477-T-G

159064821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67794507-G-A

159064822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67794508-A-T

159065190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67794919-T-C

159066595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67797188-C-T

159067163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67797470-G-A

159067433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67797717-C-T

159067610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67797892-C-T

159067634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67797916-A-G

159067887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67798132-A-G

159067897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67798142-A-G

159068234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67798479-C-T

http://identifiers.org/hco/3/GRCh38#159068239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67798484-A-C

159068453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67798693-C-T

159068456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67798696-G-A

159068675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67798917-C-G

159069056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67799270-C-G

159069268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67799481-T-G

159069437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67799650-G-A

159069437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67799650-G-T

159069463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67799675-A-G

159069597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67799818-G-A

159069597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67799818-G-T

http://identifiers.org/hco/3/GRCh38#159069736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67799955-C-A

http://identifiers.org/hco/3/GRCh38#159069795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67800012-C-A

159069795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67800012-C-T

159069850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67800082-T-A

159069850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67800082-T-C

159069896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67800128-T-C

159069896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67800128-T-G

159070043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67800265-G-A

159070043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67800265-G-T

http://identifiers.org/hco/3/GRCh38#159070121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67800343-A-C

http://identifiers.org/hco/3/GRCh38#159070155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67800379-C-A

159071135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67801328-T-C

159071444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67801628-T-C

159071702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67801882-A-G

http://identifiers.org/hco/3/GRCh38#159071795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67801977-C-A

159071863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67802036-C-T

159071916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67802089-C-T

159072104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67802264-C-T

159072175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67802327-T-C

159072239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67802382-A-G

http://identifiers.org/hco/3/GRCh38#159072626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67802820-C-A

159072714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67803058-A-G

159072872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67803204-T-A

159072884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67803216-A-G

159072884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67803216-A-T

159072899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67803234-C-T

159072995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67803328-G-A

159073029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67803360-G-A

159074868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67806184-A-T

159074910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67806231-A-G

159074910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67806231-A-T

159075068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67806381-T-A

159075331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67806640-G-T

159075564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67806972-G-A

159075809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67807256-T-C

159075932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67807339-A-G

159076735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67808191-T-C

159076903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67808353-A-T

159076988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67808437-T-C

159076988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67808437-T-G

http://identifiers.org/hco/3/GRCh38#159077081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67808523-C-A

159077272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67808684-C-T

159077366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67809287-G-A

159077786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67809608-A-T

159077788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67809610-A-G

http://identifiers.org/hco/3/GRCh38#159078070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67810090-A-C

159078121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67810125-A-T

159078157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67810161-G-C

159078242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67810245-T-C

159078458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67810457-A-G

159078516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67810472-G-A

159078574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67810510-G-C

159078698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67810626-C-T

http://identifiers.org/hco/3/GRCh38#159079131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67811244-C-A

159079131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67811244-C-G

http://identifiers.org/hco/3/GRCh38#159079139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67811252-C-A

159079576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67812121-A-G

http://identifiers.org/hco/3/GRCh38#159080077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67812850-C-A

159080077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67812850-C-T

159080315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67813190-T-A

159080593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67813465-G-A

159080593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67813465-G-T

159080706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67813578-C-T

159081602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67816299-T-C

http://identifiers.org/hco/3/GRCh38#159081632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67816329-C-A

159081719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67816414-C-T

159081748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67816443-T-C

159081797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67816493-G-T

http://identifiers.org/hco/3/GRCh38#159082005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67816762-C-A

159082108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67816863-G-A

159082108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67816863-G-T

159082152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67816903-C-G

159082197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67816944-T-C

159082264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67817024-G-A

159082296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67817056-T-C

159082441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67817205-C-G

159082486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67817266-A-G

159082486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67817266-A-T

159082556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67817346-G-A

159083030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67817922-T-G

159083116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67818004-T-A

159083427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67818304-A-G

159083698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67818528-G-C

159083913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67818773-G-A

159083924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67818784-G-A

159083924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67818784-G-C

159083932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67818790-C-G

159083932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67818790-C-T

159084226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67819042-A-G

159084236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67819052-A-T

159084289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67820505-A-G

http://identifiers.org/hco/3/GRCh38#159084382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67820580-A-C

159084532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67820741-A-G

159084630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67820838-A-G

159084820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67821030-A-G

159084821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67821031-T-C

http://identifiers.org/hco/3/GRCh38#159084822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67821032-C-A

159084823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67821033-C-T

159084847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67821056-T-C

159084850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67821059-T-A

159084868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67821079-G-A

159084881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67821090-A-G

159084907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67821116-T-C

159092877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67822823-T-C

159092995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67822937-C-T

http://identifiers.org/hco/3/GRCh38#159093107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67823052-C-A

159093157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67823105-C-T

159094530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67824429-A-G

159094569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67824467-A-G

159094585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67824483-T-C

159094851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67824741-T-G

http://identifiers.org/hco/3/GRCh38#159095010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67824885-C-A

159095166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67825018-A-G

159095170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67825022-T-C

159095209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67825062-C-T

159095237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67825090-T-A

159095321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67825564-A-G

159101517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67825703-G-C

159101635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67825791-C-G

159101684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67825836-C-G

159101767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67825916-T-C

159101831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67825982-A-G

159101900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67826046-T-A

159101968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67826113-T-C

159102106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67826244-A-G

159102122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67826260-C-T

159102136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67826274-G-T

159102457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67826609-T-C

159102724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67826800-T-C

159102813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67826891-A-G

159102929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67827091-C-T

159103081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67827244-T-C

159103161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67827319-A-T

159103195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67827349-A-G

159104203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67827608-C-T

159104306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67827707-C-T

159104359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67827759-C-T

159104362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67827762-C-T

159104600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67827943-T-G

159104675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67828011-G-A

159104850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67828584-G-A

159105197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67828874-A-G

159105306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67828989-T-C

159105344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67829024-C-T

159105589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67829270-G-A

159105806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67829481-A-G

159106333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67829951-C-T

http://identifiers.org/hco/3/GRCh38#159106392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67830010-A-C

159106408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67830025-A-G

159106501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67830136-T-C

159106539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67830168-A-G

159107811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67830526-G-A

http://identifiers.org/hco/3/GRCh38#159107892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67830621-C-A

159108004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67830718-T-A

159108004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67830718-T-G

159108046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67830747-G-A

159108046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67830747-G-T

159108171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67830854-A-G

159108362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67831049-G-A

159108745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67831803-C-T

159108789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67831845-T-C

http://identifiers.org/hco/3/GRCh38#159108889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67831962-A-C

159108926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67831989-T-C

159109035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67832095-G-A

159109179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67832241-T-C

159110114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67832528-A-G

159110304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67832707-G-A

159110580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67832957-C-T

159110727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67833095-A-G

159110941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67834792-G-C

159110972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67834829-A-G

159111016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67834873-G-A

159111043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67834904-A-G

159111089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67834950-T-G

http://identifiers.org/hco/3/GRCh38#159111252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67835134-C-A

159111307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67835205-T-C

159111307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67835205-T-G

http://identifiers.org/hco/3/GRCh38#159111530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67835733-A-C

159111566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67835763-C-T

http://identifiers.org/hco/3/GRCh38#159111721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67835925-C-A

159112766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67837395-C-T

159113145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67837723-G-C

159113252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67837831-C-T

159113277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67837856-T-A

159113390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67837969-G-A

159113395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67837974-T-C

159113461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67838040-C-T

159113468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67838047-C-G

159113561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67838140-G-A

159113697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67838275-G-A

159114058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67838636-G-T

159114656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67838916-C-T

159114839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67839084-A-T

159114900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67839145-G-C

159114908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67839153-G-T

159114999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67839230-C-T

159115298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67839527-T-C

159115347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67839575-T-A

159115347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67839575-T-G

159115494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67839683-G-A

159115505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67839694-T-A

159122256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67840571-T-C

159122553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67840859-A-G

159122662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67840981-A-G

159122843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67841168-A-G

159122859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67841184-A-G

159122891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67841216-T-C

159122910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67841235-T-C

http://identifiers.org/hco/3/GRCh38#159123191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67841506-C-A

http://identifiers.org/hco/3/GRCh38#159123387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67841563-C-A

159123447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67841622-T-C

159123476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67841657-G-A

159123512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67841691-G-T

159123650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67841818-C-G

159123693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67841862-G-C

159123809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67841966-G-A

159123912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67842073-C-T

159124022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67842172-G-A

159124174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67842315-C-T

http://identifiers.org/hco/3/GRCh38#159124177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67842318-C-A

159124181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67842320-C-T

http://identifiers.org/hco/3/GRCh38#159127233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#67842479-C-A

159127233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67842479-C-T

159127252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67842498-G-A

159127600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67842849-A-G

159127612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67842861-G-C

159127658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67842916-G-C

159127667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67842925-A-T

159127863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67843113-A-G

159127900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67843149-T-C

http://identifiers.org/hco/3/GRCh38#159128135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67843394-A-C

159128186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67843439-A-G

159128196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67843449-G-A

159128199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67843452-A-T

http://identifiers.org/hco/3/GRCh38#159128342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67843594-C-A

159128410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67843661-C-T

159128427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67843678-G-A

159128556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67843791-C-G

159128675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67843920-C-G

159129580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67844894-G-A

159129750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67845063-G-A

159129830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67845136-G-A

159129832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67845138-T-C

http://identifiers.org/hco/3/GRCh38#159131082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67847297-A-C

http://identifiers.org/hco/3/GRCh38#159131321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67847470-A-C

159131706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67847784-G-C

159131764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67847841-A-G

159131781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67847858-A-G

159132086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67848045-G-A

159132350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67849227-C-T

159132501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67849365-G-A

159132699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67849542-G-T

159132712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67849555-G-T

159132888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67849683-T-G

159132889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67849684-C-T

159133073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67849757-C-T

159133233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67849922-T-C

159133433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67850127-A-G

159133460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67850154-C-G

159133543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67850236-G-A

159133558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67850251-A-G

159133878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67853346-G-C

159133943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67853420-G-A

159133973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67853450-G-T

159134056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67853527-G-C

159134080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67853554-G-A

159134303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67853733-C-T

159134391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67853819-G-A

159134522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67853944-G-A

http://identifiers.org/hco/3/GRCh38#159134523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67853945-A-C

159134653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67854049-A-G

159134654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67854050-C-T

159134724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67854118-C-G

159134734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67854126-C-T

159135070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67854447-T-A

159135120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67854483-C-T

159135449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67854768-A-G

159135615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67854916-A-G

159135699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67854983-C-T

159135747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67855036-T-C

159135846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67855142-T-C

159135904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67855185-G-A

159135908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67855189-G-A

159135908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67855189-G-C

159135908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67855189-G-T

159136398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67855773-G-A

159136429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67855805-T-G

159136472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67855847-G-C

159136570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67855970-G-T

159136659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67856049-G-A

159136779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67856150-A-G

159136871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67856270-T-C

159136906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67856305-T-C

159137323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67856410-A-G

http://identifiers.org/hco/3/GRCh38#159137338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67856425-A-C

159137646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67856679-T-C

159138927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67857204-A-G

159138927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67857204-A-T

http://identifiers.org/hco/3/GRCh38#159138942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67857219-A-C

159138942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67857219-A-G

159138942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67857219-A-T

159139053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67857329-C-G

159139077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67857353-A-G

159139361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67857654-C-G

159141918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67859764-G-A

159141955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67859801-G-A

http://identifiers.org/hco/3/GRCh38#159142130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67859959-A-C

159142377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67860215-T-C

159143500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67860351-C-T

159143501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67860352-A-T

159143583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67860425-A-G

http://identifiers.org/hco/3/GRCh38#159143641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67860455-A-C

159144041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67860835-C-T

159144119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67860908-T-C

159144195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67860983-G-A

159144271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67861049-T-A

159144601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67861478-G-T

159144700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67861637-C-T

159144867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67861795-A-G

159144958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67861872-G-T

159145182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67862096-T-A

159145251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67862164-G-C

http://identifiers.org/hco/3/GRCh38#159145498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67862405-A-C

159145498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67862405-A-G

159145528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67862439-G-T

159145578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67862487-T-A

159145578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67862487-T-C

http://identifiers.org/hco/3/GRCh38#159145750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67862655-A-C

159145903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67862779-C-T

159145951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67862816-G-A

159146031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67862901-A-G

159146116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67862966-C-T

159146265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67863060-A-G

http://identifiers.org/hco/3/GRCh38#159146275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67863070-A-C

159146578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67863362-C-T

159146728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67864114-A-G

159147004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67864391-G-C

159147138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67864519-T-G

159147279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67864654-A-G

159147300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67864678-A-G

159147317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67864695-G-A

159147349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67864715-T-C

159147588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67864935-G-A

159148177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67866085-C-T

159148221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67866115-A-G

159148453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67866326-T-C

159148645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67866513-C-T

http://identifiers.org/hco/3/GRCh38#159148664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67866532-C-A

159148664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67866532-C-T

159148770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67866634-T-C

http://identifiers.org/hco/3/GRCh38#159148791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67866654-C-A

159148860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67866716-T-G

159148997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67866868-G-A

159149286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67867185-G-A

159149389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67867289-A-T

159149541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67867429-G-C

159149554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67867442-G-T

159149590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67867477-A-G

159149869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67867738-C-T

http://identifiers.org/hco/3/GRCh38#159149944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67867804-A-C

http://identifiers.org/hco/3/GRCh38#159151326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67868261-C-A

http://identifiers.org/hco/3/GRCh38#159151408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67868352-C-A

159151409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67868353-A-T

159151418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67868365-C-T

159151441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67868389-T-C

159151456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

159151570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67868509-C-T

159152016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67868631-C-T

159152083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67868694-C-G

159152089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67868700-G-A

159152378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67868909-A-G

159152534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67869054-C-G

159152841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67869360-A-G

http://identifiers.org/hco/3/GRCh38#159153366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67871153-C-A

159153431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67871216-T-G

159153438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67871223-G-A

159153473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67871255-G-A

159153473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67871255-G-T

159153637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67871420-G-A

159153649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67871432-T-C

159153708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67871479-A-G

159153896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67871629-A-G

159154904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67871979-C-T

159154974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67872056-G-A

159154974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67872056-G-C

159154974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67872056-G-T

159155074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67872130-C-T

159155667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67872432-A-G

159155719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67872559-C-T

159155850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67872652-T-C

159155898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67872690-C-T

http://identifiers.org/hco/3/GRCh38#159155992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67872784-C-A

159156123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67872904-A-G

159156545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67873259-T-G

159156725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67873475-C-T

159156761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67873502-T-C

159156774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67873513-G-T

159156775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67873514-G-A

159156890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67873623-G-A

159156890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67873623-G-C

159157416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67874160-T-C

159157421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67874165-A-G

159157523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67874285-C-T

159157735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67874545-A-G

159157735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67874545-A-T

159157739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67874549-A-G

159157818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67874631-A-G

159157845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67874656-A-G

159158174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67875043-T-G

159158260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67875141-G-A

159158265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67875146-T-C

159158295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67875173-C-T

159158298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67875176-C-G

http://identifiers.org/hco/3/GRCh38#159163658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67879894-C-A

159163857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67880069-C-T

159163861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67880073-A-G

159164134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67880288-C-T

159164159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67880314-T-G

159164194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67880349-G-C

159164222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67880369-A-G

159164382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67880522-C-T

159164809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67880878-C-T

159164932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67881013-C-T

159165434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67881802-G-A

159165455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67881822-T-A

159165463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67881830-A-G

159166029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67882074-C-T

159166078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67882123-C-T

159166640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67882695-T-A

159166770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67882827-G-A

159167233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67883265-A-G

159167372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67883397-C-G

159167412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67883437-G-C

159171238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67884550-T-A

159171485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67885798-G-A

159171498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67885810-G-T

159171536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67885849-T-G

159171913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67886146-A-T

159171956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67886196-A-T

159171959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67886199-A-T

159172180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67886418-T-C

159172316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67886535-A-G

http://identifiers.org/hco/3/GRCh38#159172518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67886707-A-C

159172518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67886707-A-G

159172692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67886878-T-G

159172715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67886902-G-A

159172912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67887080-T-C

159173027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67887193-T-A

159173091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67887249-T-C

159173141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67887297-G-A

http://identifiers.org/hco/3/GRCh38#159173301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67887665-C-A

159175719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67887976-A-G

159175834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67888083-G-A

159175879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67888111-C-T

159176116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67888349-A-G

159176116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67888349-A-T

159176589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67888589-T-C

159176682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67888689-T-C

http://identifiers.org/hco/3/GRCh38#159176723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67888728-A-C

159176744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67888752-C-T

159185763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67889898-G-T

159185781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67889916-C-T

159185802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67889937-A-G

159185901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67890030-A-T

159186159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67890240-T-C

159186393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67890485-G-A

159186393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67890485-G-T

http://identifiers.org/hco/3/GRCh38#159186411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67890503-C-A

http://identifiers.org/hco/3/GRCh38#159186925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67891047-C-A

159187000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67891118-C-T

159187001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67891119-A-T

159187002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67891120-T-C

159187053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67891171-G-A

159187083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67891202-T-A

159187094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67891209-A-T

159187175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67891284-T-C

159187310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67891405-T-G

159187535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67891631-G-T

159187707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67891801-A-G

159187862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67892055-C-T

159187948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67892141-G-A

159188451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67892593-C-G

159188480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67892610-T-A

159188573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67892695-G-A

159188627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67892743-C-G

159188630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67892746-G-A

159188800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67892946-A-G

159188894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67893042-G-A

159188968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67893102-C-T

159189012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67893138-G-C

159189400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67893469-A-G

159189659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67893723-A-T

159189736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67893800-G-A

159189738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67893802-C-T

159189747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67893810-G-C

159189859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67893923-T-G

159190153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67894413-G-A

159190188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67894458-A-G

http://identifiers.org/hco/3/GRCh38#159190266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67894534-A-C

159190367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67894631-T-G

159190449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67894756-T-C

159190449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67894756-T-G

http://identifiers.org/hco/3/GRCh38#159190528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#67894831-C-A

159190563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67894995-G-A

159190895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67895557-G-A

http://identifiers.org/hco/3/GRCh38#159190925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67895588-C-A

159190964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67895619-A-G

159191205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67895862-C-T

159191364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67895975-G-A

159191408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67896012-G-T

159191414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67896018-G-T

159191444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67896047-A-G

159191515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67896118-C-T

159191847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67896448-C-T

159191939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67896540-T-A

159192158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67896762-T-A

159192158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67896762-T-C

159192556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67897260-A-G

http://identifiers.org/hco/3/GRCh38#159192807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67897526-C-A

159192822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67897541-T-A

159192822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67897541-T-C

159192853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67897571-A-G

159195851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67901499-C-T

159195930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67901581-T-A

http://identifiers.org/hco/3/GRCh38#159196060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67901656-C-A

159196440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902003-A-G

159196612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902178-C-T

159196670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902246-G-A

159196770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902348-A-G

159196797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902375-G-A

159196953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902511-T-C

159196964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902522-G-A

159197014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902584-A-G

159197014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902584-A-T

159197301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902824-C-G

159197373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902913-C-T

159197375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902915-C-T

159197850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67903310-A-G

159198224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67903668-G-A

159198224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67903668-G-C

159198271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67903715-A-G

159198330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67903773-A-G

159202083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909304-C-G

159202177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909434-C-T

http://identifiers.org/hco/3/GRCh38#159202187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67909444-C-A

159202201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909453-T-C

159202291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909519-A-T

159202580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909806-G-C

159202580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909806-G-T

159202836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909895-C-T

159202889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909971-T-A

159203060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910147-G-A

159203089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910174-T-C

159203181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910292-A-G

159203194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910305-G-C

159203254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910365-G-A

159203443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910552-T-C

159203911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910846-G-A

159204035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910957-A-G

159204223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911127-G-A

159204305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911210-T-C

159204384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911277-T-C

159204408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911301-C-G

159204429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911321-C-T

159204434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911326-G-A

159204524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911409-C-T

159204651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911567-C-G

159204711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911640-C-T

159204746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911669-G-T

http://identifiers.org/hco/3/GRCh38#159204863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67911857-C-A

159204967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911932-G-A

159205119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67912071-G-T

159205133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67912085-A-T

159205135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67912087-A-G

http://identifiers.org/hco/3/GRCh38#159205140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67912092-C-A

159205140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67912092-C-G

159205166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67912118-T-C

http://identifiers.org/hco/3/GRCh38#159205225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67912169-C-A

159205225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67912169-C-T

159205368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67912301-T-C

159205412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67912333-G-T

159205415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67912336-T-C

159205469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67912391-A-T

159205553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67912439-T-G

159205621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67912504-C-G

159205667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67912556-C-G

159207326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67913954-T-C

159207478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67914105-T-C

159207590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67914214-T-C

http://identifiers.org/hco/3/GRCh38#159207738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67914353-C-A

159207738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67914353-C-G

159207801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67914420-G-T

159207816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67914435-T-C

159207971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67914577-C-T

159208393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67914945-T-C

159208460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915008-T-C

159208460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915008-T-G

159209794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915228-C-T

159209837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915267-T-C

159209879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915309-G-T

159209890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915320-G-A

159210096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915495-A-G

159210096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915495-A-T

159210133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915533-G-A

http://identifiers.org/hco/3/GRCh38#159210391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67915773-C-A

159210417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915799-G-A

159210704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915994-C-G

159211061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67916172-T-C

159211246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67916395-G-A

http://identifiers.org/hco/3/GRCh38#159211321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67916484-C-A

159211321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67916484-C-G

159211321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67916484-C-T

159211520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67916657-A-G

159211691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67916841-G-A

159212154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917255-G-A

159212168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917268-G-A

159212184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917285-C-T

159212311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917417-G-A

159212321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917427-G-A

159212348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917451-G-A

159212405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917494-G-A

159212486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917581-T-C

http://identifiers.org/hco/3/GRCh38#159212565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67917651-C-A

159212566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917652-C-T

159212610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917695-C-T

http://identifiers.org/hco/3/GRCh38#159214282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67921012-A-C

159214308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921036-C-G

159214308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921036-C-T

159214468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921188-T-A

159214606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921316-A-G

http://identifiers.org/hco/3/GRCh38#159214750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67921451-C-A

159214755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921456-G-A

159214902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921603-G-A

159214902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921603-G-T

159215022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921767-G-C

159215097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921848-C-T

159215100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921851-G-A

159215124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921871-A-G

159215428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67922153-T-A

159215428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67922153-T-C

159215453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67922179-C-T

159215651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67922406-T-C

159215963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67922714-T-A

159216084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67922847-G-A

159216084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67922847-G-T

159216993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67923748-C-T

159217029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67923779-G-A

http://identifiers.org/hco/3/GRCh38#159217133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67923864-A-C

159217133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67923864-A-G

159217159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67923875-C-G

159217159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67923875-C-T

159217409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67924125-T-A

159217485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67924159-G-T

159217606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67924256-A-G

159217700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67924586-G-A

159217752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67924696-A-G

159218093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67925028-G-A

159218425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67925401-A-G

159218516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67925479-C-G

159218612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67925569-C-T

159218687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67925626-A-T

159218796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67925731-G-T

159218847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67925782-G-C

159219063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67925966-C-G

159219063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67925966-C-T

159219310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67926198-A-T

159219400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67926275-T-C

159219560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67926411-G-A

159219852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67926710-T-G

159219880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67926732-C-T

159219992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67926832-T-C

159220262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927098-T-A

159220286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927119-A-G

159220376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927199-G-C

159220393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927216-G-A

159220429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927253-G-A

159220439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927273-G-A

159220495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927325-G-A

159220533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927356-T-C

159220593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927395-T-C

159220738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927530-T-G

159220752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927544-C-T

159220944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67928451-G-A

159221132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67929864-T-G

159221188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67929920-A-G

159221193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67929926-C-T

159226912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67937965-T-G

159227047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67938084-G-A

159227341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67938375-G-A

159227978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67938999-G-C

159228011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67939032-A-G

159228403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67939437-A-G

159229094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67939794-T-A

159229095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67939795-C-G

159229482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67940142-G-T

159229552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67940199-T-C

159229592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67940237-G-C

159233129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67940757-T-C

159233144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67940772-T-C

159233254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67940904-G-A

159235407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67942516-T-C

http://identifiers.org/hco/3/GRCh38#159235418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67942527-A-C

159235434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67942544-G-A

159235688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67942754-A-G

159235889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67942947-G-A

159235977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67943024-C-T

159236083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67943123-T-G

159236103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67943143-T-A

159236259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67943301-G-C

159236259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67943301-G-T

159236295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67943347-T-A

159236650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67943709-C-G

159236976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944033-T-G

159237365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944423-T-C

159237466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944496-C-T

159237479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944509-T-G

159237492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944522-A-G

159237514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944544-T-C

159237515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944545-A-G

159237766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944795-G-A

159237766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944795-G-T

159237823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944851-T-A

159237922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944944-G-A

159237930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944952-G-A

159237954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944989-T-C

159238418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945413-T-A

159238419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945414-A-G

159238489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945477-T-G

159238528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945517-A-G

159238654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945640-T-C

159238661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945647-C-T

159238705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945701-A-G

159238722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945721-G-A

159238861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945846-G-A

159239058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67946049-G-A

159239187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67946171-T-G

159239292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67946275-A-T

159239396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67946368-C-T

159239418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67946393-A-T

159239464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67946445-A-G

http://identifiers.org/hco/3/GRCh38#159239488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67946469-C-A

159239683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67946598-A-G

159239747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67946674-A-T

159240115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947057-G-A

159244464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947434-G-A

http://identifiers.org/hco/3/GRCh38#159244475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67947445-C-A

159244653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947619-C-T

159244802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947805-G-C

159244865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947864-G-A

159244926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947876-T-C

159245008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947959-T-A

159245013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947964-A-T

159245078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948034-A-G

159245107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948065-G-A

159245192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948169-G-A

159245308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948281-C-T

http://identifiers.org/hco/3/GRCh38#159245365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67948339-C-A

159245368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948342-T-C

159245548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948423-G-A

159245746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948434-G-A

159245746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948434-G-T

159245760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948448-A-G

159245772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948460-G-A

159245777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948465-G-A

159245777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948465-G-T

http://identifiers.org/hco/3/GRCh38#159245854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67948538-A-C

159245854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67948538-A-G

159245895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67948579-A-G

http://identifiers.org/hco/3/GRCh38#159245995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67948684-A-C

159246012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948701-G-T

159246038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948720-A-G

159246038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948720-A-T

159246048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948730-T-A

159246099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948760-C-T

159246120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948782-T-A

159246144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948803-G-A

159246304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67948955-G-A

http://identifiers.org/hco/3/GRCh38#159246318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67948970-C-A

159246374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67949160-T-C

159246585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67949428-T-G

159246693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67949523-G-C

159246693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67949523-G-T

159246711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67949541-T-C

159246712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67949542-G-A

159246751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67949585-G-A

159246770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67949604-A-G

159246924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67949734-T-C

159248431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67951153-C-T

159248736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67951421-A-G

159248779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67951469-T-A

159248779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67951469-T-C

159249295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67951689-A-G

http://identifiers.org/hco/3/GRCh38#159249316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67951713-C-A

159249316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67951713-C-T

159249328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67951731-C-T

159249394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67951797-T-C

159249405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67951808-T-G

159249525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67951955-T-C

159249812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952258-T-C

159249824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952270-C-G

159249936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952422-G-A

159249936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952422-G-T

159250288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952764-A-G

159250288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952764-A-T

159250318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952801-T-C

159250345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952837-A-G

http://identifiers.org/hco/3/GRCh38#159250875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67953083-C-A

159250875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953083-C-T

159250969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953165-A-T

159251063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953236-G-T

159251256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953402-C-T

159251521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953617-G-A

159252429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954294-C-T

159252430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954295-C-T

159252443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954308-A-G

159252578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954426-A-G

http://identifiers.org/hco/3/GRCh38#159252596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#67954444-C-A

159252596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954444-C-T

159252650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67954494-T-C

159252670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67954514-G-A

159252670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67954514-G-T

http://identifiers.org/hco/3/GRCh38#159252870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#67954718-C-A

159252870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954718-C-G

159252879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954727-T-G

159252883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954731-G-A

159252890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954740-A-T

159252891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954741-G-A

159252915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67954767-A-G

159252915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67954767-A-T

http://identifiers.org/hco/3/GRCh38#159252923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67954775-C-A

159252928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954776-T-A

159252939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954787-T-C

159252942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954790-T-A

159252942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954790-T-C

159252944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954792-T-A

159252944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954792-T-C

159252944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954792-T-G

159252951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954799-G-A

159252951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954799-G-T

159252958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67954806-G-A

159253090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67954921-G-T

159253123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67954936-A-G

159253264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955053-C-G

159253264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955053-C-T

159253323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955122-A-G

159253339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955138-A-G

159253363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955162-C-G

159253447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955247-T-C

http://identifiers.org/hco/3/GRCh38#159253763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67955507-C-A

159253763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955507-C-T

159254453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956130-C-G

159254602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956275-C-T

159254651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956569-G-C

159254889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956794-G-T

159254950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956855-G-A

159254950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956855-G-T

159255085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956969-T-C

159255140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67957020-C-T

159255162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67957041-T-C

159255275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67957147-T-G

159255491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67957367-C-G

159255491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67957367-C-T

159255572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67957451-G-A

159255572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67957451-G-T

http://identifiers.org/hco/3/GRCh38#159255741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67957610-A-C

159255840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67957682-C-T

159256804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67959251-G-A

159256815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67959263-G-A

159257152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67959613-A-G

159257170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67959648-G-C

159257383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67959844-C-T

159259030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960006-T-G

http://identifiers.org/hco/3/GRCh38#159259197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67960135-A-C

159259362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960254-C-G

159259362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960254-C-T

159259446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960347-T-G

159259455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960356-T-C

159259470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960372-C-T

159259760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960630-G-A

159259773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960643-G-A

159259841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960693-C-G

159259925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960740-T-C

159259994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960804-G-C

http://identifiers.org/hco/3/GRCh38#159260367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67961200-C-A

159260419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67961227-A-G

159260511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67961294-G-A

159260608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67961392-G-T

159260641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67961414-T-C

159261940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67961996-A-G

159261945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962001-A-G

159261984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962040-C-T

159261985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962041-C-G

159262009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962073-G-C

159262009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962073-G-T

http://identifiers.org/hco/3/GRCh38#159262171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67962230-C-A

159262177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962236-A-G

159262299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962346-A-G

159262403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962481-A-T

http://identifiers.org/hco/3/GRCh38#159262406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67962484-C-A

159262406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962484-C-T

159262443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962515-A-G

159262443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962515-A-T

http://identifiers.org/hco/3/GRCh38#159262503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67962568-A-C

159262503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962568-A-G

159262503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962568-A-T

159262564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 67962612-C-T

159262668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67962716-C-T

159262715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, missense_variant
orthologous variants: 67962763-A-G

159262805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67962852-A-G

159262894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67962940-G-T

159262951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963000-T-C

159262951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963000-T-G

http://identifiers.org/hco/3/GRCh38#159262969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67963014-A-C

159262969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963014-A-G

159263038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963069-G-T

159263064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963095-A-G

159263187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963169-A-G

159263238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963213-C-T

http://identifiers.org/hco/3/GRCh38#159263250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67963228-C-A

159263250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963228-C-G

159263250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963228-C-T

159263252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963230-G-T

159263260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963243-T-C

http://identifiers.org/hco/3/GRCh38#159263301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67963268-C-A

http://identifiers.org/hco/3/GRCh38#159263323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67963290-C-A

159263382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963340-G-A

159263382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963340-G-C

159263382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963340-G-T

http://identifiers.org/hco/3/GRCh38#159263427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67963383-A-C

159263490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963449-T-A

159263490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963449-T-C

159263523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963489-G-A

159263523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963489-G-T

159263551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963521-G-A

159263723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963655-G-T

159263743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963691-A-G

159263743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963691-A-T

159263745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67963693-A-G

159263815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67963796-G-C

159263898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67963845-G-A

159263904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67963851-C-G

159263904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67963851-C-T

159263972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67963910-T-C

http://identifiers.org/hco/3/GRCh38#159264046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67963976-C-A

159264564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67964401-C-T

159264570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67964409-G-T

159264866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67964612-G-A

159264870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67964617-T-C

159264900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67964647-G-A

159264924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67964682-T-A

159264940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67964698-T-A

http://identifiers.org/hco/3/GRCh38#159265038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67964806-A-C

159265053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67964821-A-G

159265084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67964871-T-A

159265121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67964908-G-A

http://identifiers.org/hco/3/GRCh38#159265186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67965106-A-C

159265186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron variant
orthologous variants: 67965106-A-G

159265222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, missense_variant
orthologous variants: 67965149-G-C

159265311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, missense_variant
orthologous variants: 67965226-C-T

http://identifiers.org/hco/3/GRCh38#159265371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67965283-A-C

159265371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: intron_variant, missense_variant
orthologous variants: 67965283-A-G

http://identifiers.org/hco/3/GRCh38#159265482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67965371-C-A

159265482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67965371-C-T

http://identifiers.org/hco/3/GRCh38#159265499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67965389-C-A

159265526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67965416-T-C

159265551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67965464-T-A

159265551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67965464-T-C

159265551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67965464-T-G

http://identifiers.org/hco/3/GRCh38#159265563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67965473-C-A

http://identifiers.org/hco/3/GRCh38#159265616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67965521-C-A

159265616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67965521-C-G

159265616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67965521-C-T

http://identifiers.org/hco/3/GRCh38#159265666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67965545-A-C

159265666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67965545-A-T

http://identifiers.org/hco/3/GRCh38#159265697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67965566-C-A

http://identifiers.org/hco/3/GRCh38#159265793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67965592-C-A

159265793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67965592-C-T

http://identifiers.org/hco/3/GRCh38#159265850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67965638-C-A

159265850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67965638-C-T

159266026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67965813-G-A

159266068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67965852-T-C

159266072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67965856-C-T

http://identifiers.org/hco/3/GRCh38#159266167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#67965964-C-A

159266167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32406
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67965964-C-G