107834635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49986106-C-T

107834668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49986073-G-T

107834675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49986063-G-A

http://identifiers.org/hco/3/GRCh38#107834905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49985856-A-C

107835060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49985729-G-A

107835060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49985729-G-T

107835101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49985688-T-A

107835306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 49984484-C-T

107835309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 49984481-G-A

107835370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49984420-C-T

107835689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49984058-A-G

107835811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49983942-T-C

http://identifiers.org/hco/3/GRCh38#107835876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49983882-C-A

107835876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49983882-C-T

107835982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49983781-T-C

http://identifiers.org/hco/3/GRCh38#107836710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49981710-C-A

107836710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49981710-C-T

107836711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49981709-G-A

107837825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49979300-T-G

107838452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49978724-A-G

107838453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49978723-A-T

107838981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49977955-A-G

107839655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49984420-C-T

107840445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49976870-T-A

107840449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49976866-C-T

107840503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49976815-G-A

107840894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49976458-A-G

107841195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49976161-G-A

http://identifiers.org/hco/3/GRCh38#107841208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49976148-C-A

107841208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49976148-C-T

107841209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49976147-A-G

http://identifiers.org/hco/3/GRCh38#107841220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49976135-C-A

107841220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49976135-C-T

http://identifiers.org/hco/3/GRCh38#107841229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49976127-C-A

107841243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49976113-T-C

107841294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49976026-A-T

107841495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49974841-T-C

107841496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49974840-G-T

107841527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49974810-C-T

107841672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49974679-T-C

107841834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49974518-T-C

107841853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49974499-G-A

107841853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49974499-G-T

107841854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49974498-A-T

107841954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49974058-G-A

107842247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49973754-G-T

107843584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49971528-A-T

http://identifiers.org/hco/3/GRCh38#107843655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49971460-C-A

107843776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49971347-G-C

107843776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49971347-G-T

107843809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49971318-A-T

107843837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49971287-G-A

107843927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49971209-C-G

107843927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49971209-C-T

107843952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49971184-C-T

http://identifiers.org/hco/3/GRCh38#107843959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49971177-C-A

107843959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49971177-C-T

107843960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49971176-C-T

107843986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49971146-A-G

107844452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49970557-G-A

http://identifiers.org/hco/3/GRCh38#107844724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49970284-A-C

107844748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49970255-T-C

107844963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49970047-A-G

107845051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49969962-T-C

107845199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49969834-T-C

107845199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49969834-T-G

107845392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49969460-T-A

107845412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49969440-T-G

107845442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49969410-T-C

107845447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49969405-C-G

107845512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49969352-C-T

107845554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49969299-G-T

107845558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49969295-T-C

107845958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49968878-G-A

107845965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49968870-G-A

107845966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49968869-G-A

107846396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49968488-T-A

107846396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49968488-T-C

107846396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49968488-T-G

107846400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49968484-G-A

107846512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49968358-T-C

http://identifiers.org/hco/3/GRCh38#107846993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49967845-A-C

107847574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49967245-C-T

107847747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49966860-G-T

http://identifiers.org/hco/3/GRCh38#107847802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49966805-C-A

107847809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49966798-C-T

http://identifiers.org/hco/3/GRCh38#107848002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49966634-A-C

107848004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49966632-T-A

107848109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49966522-A-G

107848190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49966432-T-A

http://identifiers.org/hco/3/GRCh38#107848394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49966217-A-C

107848500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49966103-C-G

107848514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49966089-T-G

107848518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49966085-C-T

http://identifiers.org/hco/3/GRCh38#107848542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49966057-C-A

107848542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49966057-C-T

107848580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49966019-G-T

http://identifiers.org/hco/3/GRCh38#107848739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49965864-C-A

107848739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49965864-C-T

107848867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49965752-G-T

107848887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49965734-C-T

107848891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49965730-T-C

107848908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49965713-G-T

107848934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49965662-G-T

107848971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49965625-A-G

http://identifiers.org/hco/3/GRCh38#107849042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49965538-A-C

107849042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49965538-A-G

107849113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49965466-G-A

107849113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49965466-G-T

107849374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49965202-G-A

107849476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49965101-G-A

107849538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49965044-T-G

107849747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49964845-T-C

107850022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49964578-G-A

107850059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49964533-A-T

http://identifiers.org/hco/3/GRCh38#107850064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49964528-A-C

http://identifiers.org/hco/3/GRCh38#107850065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49964527-C-A

107850065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49964527-C-T

107850074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49964518-T-C

107850223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49960707-G-T

107850411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49960396-G-A

107850411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49960396-G-T

http://identifiers.org/hco/3/GRCh38#107850531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49960182-C-A

http://identifiers.org/hco/3/GRCh38#107850569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49960128-A-C

107850583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49960057-G-A

107850583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49960057-G-T

http://identifiers.org/hco/3/GRCh38#107850601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49960039-C-A

107850632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49960008-G-T

107850731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49959905-G-A

107850935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49959706-A-G

107851912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49959541-G-A

107851914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49959539-T-G

http://identifiers.org/hco/3/GRCh38#107851969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49959485-C-A

107853420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49951228-C-T

107853437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49951205-G-C

107853783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49949692-T-G

107854196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49949278-A-T

107854525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49948696-A-T

107854623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49948612-C-T

107854625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49948610-T-C

107854641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49948595-C-T

107854642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49948594-G-A

107854642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49948594-G-C

107854647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49948589-C-T

107854660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49948580-G-A

107854660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49948580-G-C

107854660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49948580-G-T

107854829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49948428-T-C

107855051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49948206-G-A

107855051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49948206-G-T

107855141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49948135-G-T

107855340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49947938-A-G

107855340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49947938-A-T

107855343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49947935-G-A

107855413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49947864-G-C

107855513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49947769-G-A

107855540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49947734-G-A

107855665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49947628-G-A

107856197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49947570-G-A

107856197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49947570-G-T

107856199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49947568-C-G

http://identifiers.org/hco/3/GRCh38#107856203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49947564-C-A

107856203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49947564-C-T

107856207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49947560-A-G

107856239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49947527-G-A

107856239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49947527-G-T

http://identifiers.org/hco/3/GRCh38#107856325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#49947436-C-A

http://identifiers.org/hco/3/GRCh38#107856417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49947345-C-A

http://identifiers.org/hco/3/GRCh38#107856420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49947342-C-A

107856794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49947004-G-A

107856815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49946983-A-G

107856815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49946983-A-T

107856821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49946924-G-A

107856951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49946757-T-A

107856969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49946736-A-G

107856986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49946719-G-T

107857147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49946559-A-G

http://identifiers.org/hco/3/GRCh38#107857155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49946551-C-A

107857172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49946534-C-T

http://identifiers.org/hco/3/GRCh38#107857188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49946520-C-A

107857256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49946452-T-C

http://identifiers.org/hco/3/GRCh38#107857557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49945999-C-A

107857569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49945987-T-A

http://identifiers.org/hco/3/GRCh38#107857657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49945911-C-A

107857753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49945825-C-T

107857893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49945688-G-T

107858951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49945009-A-G

107859038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49944922-A-G

107859117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49944840-T-C

107859148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49944804-G-T

107859208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49944742-A-G

107859210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49944740-G-A

http://identifiers.org/hco/3/GRCh38#107859227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49944723-C-A

107859976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49944380-C-G

107859981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49944375-G-A

107859996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49944359-A-G

107860222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49944183-G-A

107860407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49944099-C-T

http://identifiers.org/hco/3/GRCh38#107860504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49944014-C-A

107860504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49944014-C-T

107860579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49943955-A-T

107860581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49943953-C-T

107861461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49943779-A-G

107861534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49943703-G-C

107869244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49937401-T-G

http://identifiers.org/hco/3/GRCh38#107869507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49937185-C-A

107869507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49937185-C-T

107869525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49937168-C-G

107869683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49937027-C-G

107869827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49936884-C-T

http://identifiers.org/hco/3/GRCh38#107869895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49936816-C-A

107869962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49936762-T-C

http://identifiers.org/hco/3/GRCh38#107870433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49936331-C-A

107870464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49936303-G-A

107870771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49935556-T-G

107870837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49935490-A-G

http://identifiers.org/hco/3/GRCh38#107871085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49935241-C-A

107871085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49935241-C-T

107871215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49935049-A-G

107873432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49934704-G-C

107873944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49934507-C-T

107873989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49934458-G-A

107874060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49934387-G-A

http://identifiers.org/hco/3/GRCh38#107874162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49934286-A-C

107875046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49930774-T-C

107875916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49928608-A-G

107876282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49928233-T-C

107876287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49928228-C-T

107876291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49928224-C-T

107876304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49928214-A-G

107876325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49928193-A-G

107876354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49928161-A-T

107876376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49928142-G-T

http://identifiers.org/hco/3/GRCh38#107876444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49928080-C-A

107876744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49927729-A-G

107876864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49927557-T-C

107877481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49926383-A-G

107877509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49926357-T-C

107877536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49926330-T-C

107877664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49926219-T-G

107878091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49924091-A-G

107878136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49924045-C-G

107878149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49924032-T-C

http://identifiers.org/hco/3/GRCh38#107878190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49923991-C-A

107878349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49923854-T-C

http://identifiers.org/hco/3/GRCh38#107878481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49923730-C-A

107878777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49923477-C-G

107878877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49923392-C-G

107878894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49923375-T-A

107879143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49923152-T-A

107879144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49923151-T-C

107879516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49922773-G-T

107879544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49922747-A-G

107879702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49922593-G-A

107879771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49922533-T-C

107882545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49918412-T-C

107882804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49917130-A-T

107883043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49916887-G-A

107883218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49916753-A-G

http://identifiers.org/hco/3/GRCh38#107883267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49916700-C-A

107883267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49916700-C-T

http://identifiers.org/hco/3/GRCh38#107883271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49916697-C-A

107883271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49916697-C-T

107883315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49916657-T-C

107883413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49916561-C-T

107883516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49916454-C-T

107883637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49916364-T-C

107883652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49916349-G-T

107883764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49916230-G-A

107884469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49915517-A-G

107884498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49915488-G-C

107884638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49915350-T-A

107884682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49915306-G-C

107884918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49915067-C-G

107884920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49915065-T-G

107884928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49915056-C-T

107885117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49914798-G-T

http://identifiers.org/hco/3/GRCh38#107885250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49914681-C-A

http://identifiers.org/hco/3/GRCh38#107885478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49914455-A-C

107885505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49914426-C-T

107885509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49914422-G-A

107885627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49914342-C-T

http://identifiers.org/hco/3/GRCh38#107889520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49913468-A-C

107889520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49913468-A-G

107890329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49912536-C-T

107890412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49912413-A-G

107890775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49912082-A-T

107891198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49911951-C-G

107891298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49911845-T-C

http://identifiers.org/hco/3/GRCh38#107891820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49910406-A-C

107891917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49910322-G-T

107892086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49910159-G-A

107892724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49904951-G-A

107892782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49904888-G-A

107892782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49904888-G-T

107893169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49903898-G-A

107893567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49903515-G-A

107893616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49903439-T-G

107894038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49902919-T-C

107894933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49901207-A-G

107895273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49900890-T-C

107895294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49900869-C-T

107895682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49900149-G-A

107895844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49899996-G-A

107896290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49899511-T-C

107896423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49899377-G-A

107896506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49899281-A-G

107896507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49899280-T-C

http://identifiers.org/hco/3/GRCh38#107896534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49899253-C-A

107896534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49899253-C-T

http://identifiers.org/hco/3/GRCh38#107896580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49899218-C-A

107896612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49899187-A-T

107896672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49899122-A-G

107897493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49896695-T-C

107897697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49896492-G-T

107897705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49896484-A-G

107897902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49896248-T-G

107898187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49895998-A-G

107898255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49895908-C-G

107898548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49895635-C-T

107898903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49894874-T-C

107898940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49894830-T-C

107898941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49894829-A-G

107898993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49894781-T-C

107899010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49894764-T-C

http://identifiers.org/hco/3/GRCh38#107899087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49894681-A-C

107899087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49894681-A-G

107899088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49894680-T-A

107899296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49894510-C-T

107899541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49894276-G-T

107899633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49894184-A-G

107899752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49894075-C-T

107899799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49894030-T-C

107899925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49893902-C-G

107900101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49893731-T-A

107900101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49893731-T-C

107900118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49893711-G-A

107900118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49893711-G-C

107900127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49893707-T-G

107900160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49893691-G-A

107900170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49893680-A-T

http://identifiers.org/hco/3/GRCh38#107900254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49893596-A-C

107900390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49893435-G-A

107900630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49892927-T-C

107900662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49892895-T-G

107900700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49892865-G-C

107900700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49892865-G-T

107900727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49892841-G-A

107901012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49892573-C-T

107901361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49892031-C-T

107901528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49891917-T-C

107901561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49891887-C-T

107901659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49891807-T-C

107904247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49890257-T-C

107904282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49890224-T-C

107905185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49889674-C-T

107905314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49889551-C-T

107905388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49889471-G-A

107905388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49889471-G-C

107905475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49889395-T-C

107905780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49889143-G-A

107905810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49889110-T-C

107906198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49886346-C-T

107908093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49885617-T-C

107908217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49885516-T-A

107908392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49885347-G-A

107910498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49884616-G-A

107910498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49884616-G-C

107910498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49884616-G-T

http://identifiers.org/hco/3/GRCh38#107910945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49884167-A-C

http://identifiers.org/hco/3/GRCh38#107910978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49884140-C-A

http://identifiers.org/hco/3/GRCh38#107911136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49883989-A-C

107911187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49883932-A-G

107911224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49883885-A-G

107911233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49883876-C-G

107911392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49883692-T-G

107911422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49883663-G-A

107911717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49883444-A-T

107911789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49883372-G-A

107911832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49883329-T-C

107912102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49883071-C-T

107912180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49882996-A-G

107912239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49882939-A-G

107912432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49882094-G-A

107913551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49880285-A-G

107913624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49880147-C-G

107913673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49880115-C-G

107913917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49879882-A-G

107913923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49879876-A-G

107915360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49878431-G-T

107915437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49878370-G-A

107915873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49876741-G-A

107916019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49876595-T-C

107916109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49876506-C-T

107916241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49876352-C-T

107916290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49876305-T-C

107916774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49875877-A-G

107916783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49875868-G-T

107916841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49875810-G-C

107917110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49875522-A-G

107917110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49875522-A-T

107917205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49875450-T-C

107917208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49875447-T-C

107917250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49875405-G-C

107917325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49875336-G-A

107918163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49875020-A-G

107918602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49874707-T-C

107918787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49874489-C-G

107918938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49874345-A-G

107918938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49874345-A-T

107919322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49873944-C-T

107919403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49873863-C-T

107919550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49873769-A-G

107919771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49873485-C-T

107920287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49872722-G-C

http://identifiers.org/hco/3/GRCh38#107920603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49872432-A-C

107920805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49872240-A-G

107920895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49871773-G-T

107920983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49871690-A-T

107921139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49871399-A-G

107921185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49871355-G-A

107921212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49871327-A-G

107921259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49871187-G-T

107921412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49870998-G-A

107921412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49870998-G-C

107921444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49870968-G-A

107921444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49870968-G-T

http://identifiers.org/hco/3/GRCh38#107921753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49870721-C-A

107922034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49870503-G-A

107923885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49870306-C-T

107924060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49870150-T-C

107924181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49870037-T-G

107924230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49869987-T-C

107925912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49869589-A-G

http://identifiers.org/hco/3/GRCh38#107925923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49869578-C-A

107925986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49869511-A-G

107925998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49869499-A-T

107926469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49869045-C-G

107926528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49868992-C-G

107926528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49868992-C-T

107926601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49868926-C-T

107926617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49868909-T-C

107926963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49867482-G-A

107927006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49867375-C-G

107927318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49866929-T-A

107927453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49866816-G-T

107927486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49866783-G-A

107927524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49866744-C-G

107927529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49866739-C-T

http://identifiers.org/hco/3/GRCh38#107927590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49866678-C-A

107927743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49866531-G-A

107927743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49866531-G-C

http://identifiers.org/hco/3/GRCh38#107927850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49866424-C-A

107927850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49866424-C-T

107927916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 49866358-G-A

107927916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 49866358-G-T

107927956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 49866323-G-A

107927956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 49866323-G-T

107928185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49866074-G-A

107928185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49866074-G-T

107928198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 49866061-G-T

107928322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49865938-T-A

107928322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49865938-T-C

http://identifiers.org/hco/3/GRCh38#107928330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49865930-A-C

107928330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49865930-A-G

107928411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 49865794-A-G

107928492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49865754-C-G

107928492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49865754-C-T

http://identifiers.org/hco/3/GRCh38#107928557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#49865698-C-A

107928578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49865677-G-C

107928578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49865677-G-T

http://identifiers.org/hco/3/GRCh38#107928588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49865667-C-A

107928588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49865667-C-G

107928588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49865667-C-T

http://identifiers.org/hco/3/GRCh38#107928592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49865592-A-C

107928592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49865592-A-G

107928620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49865511-C-T

http://identifiers.org/hco/3/GRCh38#107928621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49865510-C-A

107928621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: 49865510-C-T

http://identifiers.org/hco/3/GRCh38#107928842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27702
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49865313-A-C