46293671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non coding transcript exon variant
orthologous variants: 87057724-G-A

46293749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non coding transcript exon variant
orthologous variants: 87057785-C-T

46293807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non coding transcript exon variant
orthologous variants: 87057842-T-A

46293807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non coding transcript exon variant
orthologous variants: 87057842-T-C

46293810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non coding transcript exon variant
orthologous variants: 87057845-G-T

46293851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non coding transcript exon variant
orthologous variants: 87057885-G-A

46293966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non coding transcript exon variant
orthologous variants: 87058021-G-T

46294006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non coding transcript exon variant
orthologous variants: 87058061-T-C

46294032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non coding transcript exon variant
orthologous variants: 87058088-G-A

46294032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non coding transcript exon variant
orthologous variants: 87058088-G-T

46294086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non coding transcript exon variant
orthologous variants: 87058142-T-C

46294260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87058484-G-A

46294265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87058489-T-A

46294265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87058489-T-C

46294424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87058650-G-A

46296268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87059959-C-G

46296323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060015-G-C

46296326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060018-C-G

46296327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060019-C-T

46296363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060049-G-T

46296385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060072-G-A

46296415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060100-A-G

46296603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060231-C-G

http://identifiers.org/hco/2/GRCh38#46296651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87060293-C-A

46296651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87060293-C-T

http://identifiers.org/hco/2/GRCh38#46296737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87060377-C-A

46296758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060397-A-T

46296770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060409-G-A

46296861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060521-A-G

46297073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060775-C-G

46297073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060775-C-T

46297099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060798-C-T

46297154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060851-G-A

46297174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060871-G-A

46297174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87060871-G-C

http://identifiers.org/hco/2/GRCh38#46297306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87061016-A-C

46297306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87061016-A-G

http://identifiers.org/hco/2/GRCh38#46297309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87061019-C-A

46297309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87061019-C-G

46297318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87061027-G-A

http://identifiers.org/hco/2/GRCh38#46297560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87061290-A-C

46297717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87061503-T-C

46297827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87061616-G-T

46297880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87061687-G-A

46297932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87061731-G-A

46297932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87061731-G-C

http://identifiers.org/hco/2/GRCh38#46297973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87061772-C-A

46297973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87061772-C-G

46297973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87061772-C-T

46298031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87061830-G-T

46298089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87061888-T-A

46298089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87061888-T-C

46298089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87061888-T-G

46298252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87062030-G-A

46298252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87062030-G-C

46298252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87062030-G-T

46298295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87062070-C-G

46298365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87062137-G-A

46298443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87062212-A-G

46298720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87062464-G-A

46298824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87062571-G-A

46298835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87062582-G-A

46298835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87062582-G-C

46299031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87062762-G-T

46299277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87062962-G-C

46299301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87062989-G-A

46299310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87062998-T-A

46299603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87063201-T-C

46299815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87063374-G-A

46299946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87063497-G-A

46299946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87063497-G-T

46299988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87063542-G-C

46300058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87063591-T-C

http://identifiers.org/hco/2/GRCh38#46300099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87063624-A-C

46300401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87063873-G-A

46300401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87063873-G-C

46300575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87063976-C-G

46300890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87064288-C-G

46300952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87064344-G-T

46301137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87064569-T-G

46301705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87064835-G-C

46301901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87065019-T-C

46302060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87065242-A-G

46302145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87065334-T-G

46302180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87065347-A-G

46302180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87065347-A-T

46302223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87065383-T-A

46302542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87065698-C-T

46303401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87066344-G-T

http://identifiers.org/hco/2/GRCh38#46303519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87066456-C-A

46303820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87066740-G-C

http://identifiers.org/hco/2/GRCh38#46303946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87066791-C-A

46303946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87066791-C-T

46303995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87066845-C-G

46304227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87067052-T-A

http://identifiers.org/hco/2/GRCh38#46305240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87068013-C-A

46305240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87068013-C-T

46305298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87068067-C-T

46305569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87068276-G-A

http://identifiers.org/hco/2/GRCh38#46305626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87068561-A-C

46305626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87068561-A-G

46305829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87068740-G-A

46305878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87068824-G-A

46305878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87068824-G-T

46306230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87069168-T-C

46306348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87069246-G-C

46306828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87069702-T-C

46307093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87070004-T-C

46307418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87070320-G-C

46307480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87070384-C-T

46307625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87070535-A-T

46307653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87070551-G-A

http://identifiers.org/hco/2/GRCh38#46307698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87070591-A-C

46307889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87070737-G-A

46307905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87070755-C-G

46307948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87070792-A-G

46307992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87070837-C-G

46308067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87070908-C-T

46308768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87071676-C-T

46308786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87071694-G-A

46309163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87071953-A-G

46309252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072046-A-G

46309299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072092-G-A

46309299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072092-G-C

46309552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072325-A-G

46309586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072352-G-A

46309633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072396-G-C

46309694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072454-G-A

46309794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072549-T-A

http://identifiers.org/hco/2/GRCh38#46309816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87072571-A-C

46309817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072572-T-C

46309876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072605-G-C

46309929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072654-C-G

http://identifiers.org/hco/2/GRCh38#46309970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87072694-C-A

46310062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072771-A-G

46310092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072801-C-T

46310151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072851-C-T

46310172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072873-A-G

46310180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072881-C-T

46310187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072888-C-T

46310188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87072889-C-T

http://identifiers.org/hco/2/GRCh38#46310357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87072990-A-C

http://identifiers.org/hco/2/GRCh38#46310447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87073070-C-A

46310474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87073096-G-A

46310602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87073205-T-C

46310823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87073421-A-G

46310834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87073432-G-C

46310924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87073507-T-C

46311654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87074141-C-T

http://identifiers.org/hco/2/GRCh38#46311722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87074200-C-A

46311759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87074264-C-T

46311872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87074369-G-A

46312007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87074478-A-T

46312036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87074498-G-A

46312164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87074613-G-A

46312872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075227-G-T

46312913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075265-T-G

46313293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075537-C-T

46313375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075619-C-T

46313526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87075746-A-T

http://identifiers.org/hco/2/GRCh38#46313566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87075770-C-A

46314426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87076382-A-G

46314722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87076677-G-C

46314997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87076911-G-A

46315284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87077171-C-T

46316052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87077953-G-A

46316086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87077989-T-C

46316105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87078008-G-T

46318973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87078073-G-A

46319272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87078331-C-T

46319355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87078410-A-G

46319484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87078534-T-G

46319557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87078596-A-G

46319720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87078748-C-G

46319720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87078748-C-T

http://identifiers.org/hco/2/GRCh38#46319913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87079158-A-C

46319947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87079197-C-T

46320065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87079304-A-G

46320234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87079470-G-C

46320277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87079519-T-C

46320277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87079519-T-G

http://identifiers.org/hco/2/GRCh38#46320334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87079580-A-C

46320515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87079761-T-C

46320596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87079839-C-T

46320841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87080078-G-A

46322572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87080608-T-A

46322620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87080657-C-G

46322620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87080657-C-T

46322773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87080784-C-G

46322773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87080784-C-T

46322814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87080827-C-G

46322948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87080944-T-G

46323150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87081144-C-T

46323230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87081228-G-A

46323230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87081228-G-T

46323246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87081244-C-T

46323377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87081348-C-T

http://identifiers.org/hco/2/GRCh38#46323378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87081349-C-A

46323378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87081349-C-T

http://identifiers.org/hco/2/GRCh38#46323388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87081358-C-A

46323422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87081392-T-A

46323422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87081392-T-G

46323617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87081423-A-G

46324071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87081834-G-T

46324142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87081963-C-T

46324636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87082477-C-T

46324691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87082554-C-T

46324856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87082718-C-T

46325120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87082970-C-T

46325149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87082999-C-T

46325188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87083042-G-C

46325205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87083058-T-A

46325273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87083126-G-A

46325420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87083260-G-T

46325576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87083412-G-A

46326130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87083901-G-A

46326249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87084006-T-C

46326305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87084043-T-C

46326374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87084097-G-A

46326479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87084190-A-T

http://identifiers.org/hco/2/GRCh38#46326707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87084388-A-C

46326737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87084417-G-C

46326843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87084494-T-G

46327081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87084714-G-T

46327311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87084928-G-A

46327812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87085758-G-C

46327962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87085913-A-T

46327986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87085937-G-A

46327990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87085941-T-C

46328256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87086126-A-G

http://identifiers.org/hco/2/GRCh38#46328315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87086184-A-C

46328504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87086795-G-A

46328604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87086883-G-A

46328613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87086892-C-G

46328703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87086968-G-A

46328703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87086968-G-T

46328821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87087056-T-C

46329091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87087295-G-C

46329236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87087432-G-A

46329422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87087590-G-A

46330783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87088552-C-T

46332018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87089767-A-G

46332094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87089817-C-T

46332108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87089835-C-T

46332138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87089864-T-C

46332139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87089865-G-C

46332183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87089906-C-G

46332183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87089906-C-T

http://identifiers.org/hco/2/GRCh38#46332432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87090112-A-C

46332807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87090492-T-C

46332922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87090579-G-A

46333096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87090734-T-G

http://identifiers.org/hco/2/GRCh38#46333238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87090876-C-A

46333249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87090887-T-A

46333249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87090887-T-C

46333373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091040-T-C

46333447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091113-G-A

46333473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091139-G-A

46333473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091139-G-T

http://identifiers.org/hco/2/GRCh38#46333501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87091158-A-C

http://identifiers.org/hco/2/GRCh38#46333551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87091207-A-C

46333636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091249-G-A

46333988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091395-A-G

46334167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091570-A-G

http://identifiers.org/hco/2/GRCh38#46334271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87091591-C-A

46334581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091838-G-T

46334634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091884-G-C

46334634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091884-G-T

46334704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87091948-T-C

46335129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87092474-T-G

46335216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87092549-G-A

46335356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87092711-A-G

46335458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87092799-C-G

46335729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87093078-G-A

46335729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87093078-G-T

46335779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87093130-C-T

46335819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87093171-G-T

46336154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87093532-C-T

46336186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87093566-G-A

46336457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87093787-G-A

46336457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87093787-G-C

46336700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87093923-T-G

46336935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87094132-A-G

46336987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87094209-G-C

46337154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87094365-T-C

46337183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87094399-G-C

http://identifiers.org/hco/2/GRCh38#46337330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87094521-A-C

46337673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87094856-A-G

http://identifiers.org/hco/2/GRCh38#46337761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87094942-C-A

46337953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87095225-G-A

46338087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87095362-G-C

http://identifiers.org/hco/2/GRCh38#46338156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87095428-A-C

46338484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87095749-G-A

46338539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87095793-C-T

46338775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87095986-G-T

46339071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87096185-G-A

46339120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87096236-G-A

http://identifiers.org/hco/2/GRCh38#46339232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87096343-C-A

46339277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87096388-A-G

46339338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87096405-T-C

46339420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87096462-A-G

46339649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87096660-G-A

46339712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87096716-T-C

46339713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87096717-G-C

46339745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87096749-C-T

46339746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87096750-A-T

46339769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87096772-C-T

http://identifiers.org/hco/2/GRCh38#46339770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87096773-A-C

46339863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87096863-C-T

46339870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87096870-C-T

46339970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87096914-G-A

46340047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87096975-G-A

46340110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87097035-T-G

46340450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87097360-A-T

46340604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87097446-C-G

46340604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87097446-C-T

46340656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87097497-T-C

46340703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87097531-A-G

46341228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87097748-C-T

46341436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87097959-C-T

46341498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87098025-G-A

46341500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87098027-A-G

46341501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87098028-T-A

http://identifiers.org/hco/2/GRCh38#46341575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87098093-C-A

46341828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87098339-T-C

46341831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87098344-T-G

46341952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87098468-C-T

46342518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099544-A-G

46343376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87100599-T-A

46343452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87100667-A-G

46344059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102164-G-A

46344176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102274-T-C

46344259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102385-T-C

46344288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102399-C-G

46344288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102399-C-T

http://identifiers.org/hco/2/GRCh38#46344403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87102503-C-A

46344403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102503-C-T

46344404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102504-G-A

46344433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102533-G-C

46344724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102817-G-A

46344879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102961-G-A

46345047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103134-C-T

46345102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103197-G-C

46345113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103208-C-G

46345242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103235-T-A

46345310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103263-A-G

46345331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103284-A-G

46345496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103415-A-T

46345531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103441-C-T

46345616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103517-G-T

46345717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103635-G-T

46345750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103665-T-C

46345865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103753-C-T

46345972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103836-A-G

46346011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103869-G-A

46346071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103906-C-T

46346134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103968-G-A

46346164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104000-C-T

46346671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104358-T-C

46346758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104438-A-G

46346774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104453-G-A

46346793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104466-G-T

46346816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104487-G-C

46346845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104515-C-T

46346846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104516-G-A

46346846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104516-G-T

46346867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87104538-A-T

46346906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87104577-G-A

46346912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87104583-T-C

46347113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104857-A-T

46347120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104864-T-G

http://identifiers.org/hco/2/GRCh38#46347229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87105023-C-A

46347229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105023-C-G

46347229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105023-C-T

46347285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87105077-G-A

46347285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87105077-G-T

46347325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87105143-A-G

46347328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87105146-G-T

46347333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87105151-G-T

46347355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87105173-C-G

46347355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87105173-C-T

46347493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87105301-T-C

46347493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87105301-T-G

http://identifiers.org/hco/2/GRCh38#46347625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87105410-C-A

46347665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105471-G-A

46347665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105471-G-C

http://identifiers.org/hco/2/GRCh38#46347667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87105473-C-A

http://identifiers.org/hco/2/GRCh38#46347678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87105500-C-A

46347678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105500-C-T

46347847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105673-G-A

46347847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105673-G-C

46347847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105673-G-T

46347991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105806-C-T

46348107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105919-G-A

46348143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105955-G-A

46348156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105968-C-G

46348176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105988-C-G

46348176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105988-C-T

46348342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87106178-C-T

46348371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87106208-G-T

46349260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87106489-C-T

46349455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87106671-G-A

http://identifiers.org/hco/2/GRCh38#46349463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87106673-C-A

http://identifiers.org/hco/2/GRCh38#46349554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87106753-C-A

46349693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87106877-G-T

46349788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87106961-G-T

46349879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87107701-G-C

46349937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87107762-C-T

46350157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87107879-C-G

46350168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87107890-T-C

46350184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87107905-C-T

46350368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108043-T-C

46350593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108267-G-A

46350593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108267-G-T

46350720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108386-A-G

46350800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108465-G-A

46350800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108465-G-C

46350887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108579-T-C

46350887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108579-T-G

http://identifiers.org/hco/2/GRCh38#46350902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87108594-C-A

46350902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108594-C-T

46351198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108873-C-T

46351312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108986-T-C

46351561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87109195-G-A

46351561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87109195-G-T

46351800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87109364-T-C

46351964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87109516-G-A

46352462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87109950-G-A

46352536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87109973-G-A

46352536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87109973-G-T

http://identifiers.org/hco/2/GRCh38#46352539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87109976-C-A

46352545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87109982-G-A

46352741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110168-C-T

46352859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110281-G-A

46353011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110430-A-G

46353011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110430-A-T

46353028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110446-G-A

46353089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110507-T-C

46353158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110568-G-A

46353397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110828-C-T

46353498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110922-G-A

46353498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110922-G-T

46354390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87111094-A-G

46354514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87111183-G-T

46354561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87111221-A-G

46354632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87111277-G-T

46354747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87111385-T-G

46354867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87111494-C-T

http://identifiers.org/hco/2/GRCh38#46354987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87111637-C-A

46355076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87111827-C-T

http://identifiers.org/hco/2/GRCh38#46355370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87112119-C-A

46355622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112374-C-T

http://identifiers.org/hco/2/GRCh38#46355863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87112398-C-A

46355863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112398-C-G

46356004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112504-G-A

46356004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112504-G-T

46356007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112507-G-T

http://identifiers.org/hco/2/GRCh38#46356057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87112543-C-A

46356057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112543-C-T

http://identifiers.org/hco/2/GRCh38#46356092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87112566-A-C

46356092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112566-A-T

46356102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112576-G-A

46356102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112576-G-C

46356102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112576-G-T

46356185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87112655-C-G

46356185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87112655-C-T

46356245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87112715-A-G

46356248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87112718-T-C

46356248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87112718-T-G

46356299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87112769-A-G

46356308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112778-A-G

46356353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112822-G-A

46356354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112823-T-C

46356371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112840-T-A

46356371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112840-T-C

46356380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112849-C-T

http://identifiers.org/hco/2/GRCh38#46356387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87112856-A-C

http://identifiers.org/hco/2/GRCh38#46356398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87112867-C-A

http://identifiers.org/hco/2/GRCh38#46356405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87112874-A-C

46356405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112874-A-G

46356415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112883-G-T

http://identifiers.org/hco/2/GRCh38#46356425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87112893-C-A

46356425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112893-C-T

46356435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112903-G-A

46356435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112903-G-T

46356566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113023-C-T

46356674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113133-T-C

46356891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113335-A-G

46356930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113368-T-A

46356930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113368-T-G

46356939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113374-T-A

46357317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113713-G-A

http://identifiers.org/hco/2/GRCh38#46357453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87113804-C-A

46357527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113891-G-A

46357610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113969-T-C

46357639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113982-G-A

http://identifiers.org/hco/2/GRCh38#46357655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87113998-C-A

46357688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87114030-C-G

46358247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87114600-A-G

46358400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87114736-A-G

46359294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87115318-G-A

46359294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87115318-G-C

46359306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87115330-T-A

46359306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87115330-T-G

46359335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87115359-A-T

46359385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87115409-C-G

46359496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87115497-T-A

46359545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87115514-A-T

46359568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87115533-T-C

46359959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87115890-G-A

46360158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87116164-G-T

46360509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87116687-G-A

http://identifiers.org/hco/2/GRCh38#46360604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87116763-C-A

46360708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87116856-G-A

46360708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87116856-G-C

46360807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87116937-G-A

46360807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87116937-G-C

http://identifiers.org/hco/2/GRCh38#46360836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87116965-A-C

46360841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87116970-C-T

http://identifiers.org/hco/2/GRCh38#46360866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87116993-C-A

46360941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87117068-T-A

46361124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87117234-A-G

46362772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87116564-T-C

46363168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87117841-T-A

46363168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87117841-T-C

46363255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87117904-A-G

46363277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87117929-T-G

http://identifiers.org/hco/2/GRCh38#46363359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87117983-C-A

46363391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87118005-T-C

46363632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87118219-T-C

46363677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87118265-C-T

46363848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, undefined
orthologous variants: 87118430-G-A

46363952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, undefined
orthologous variants: 87118517-G-A

46364075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, undefined
orthologous variants: 87118618-G-A

http://identifiers.org/hco/2/GRCh38#46364296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87118879-A-C

46364308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87118885-G-A

46364308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87118885-G-T

46364615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87119165-T-A

46364615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87119165-T-C

46364647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87119215-A-G

46364662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87119229-G-A

46365016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87119691-C-G

46365038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87119707-G-T

46365039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87119708-G-C

46365039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87119708-G-T

46365258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87119863-T-G

46365589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87121105-T-C

46365796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87121308-G-T

46365944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87121438-A-G

46366060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87121554-G-T

46366097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87121625-G-A

46366097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87121625-G-T

46366130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87121698-A-G

46366132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87121700-C-T

46366220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87121838-G-A

46366272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87121901-C-T

46366342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87122155-T-C

46366364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87122177-C-T

46366459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87122245-A-G

46366501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87122289-T-C

46366643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87122405-G-A

46366714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87122472-G-A

46366729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87122480-A-T

http://identifiers.org/hco/2/GRCh38#46366778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87122531-A-C

46366851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87122576-G-A

46366972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87122697-A-G

http://identifiers.org/hco/2/GRCh38#46367180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87122904-A-C

46367193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87122919-A-G

46367480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87123167-A-G

46367774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87123385-T-C

46367775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87123386-T-C

46367810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87123421-C-G

46367810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87123421-C-T

46367913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87123545-G-A

46367979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87123603-C-G

46367979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87123603-C-T

46368516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87123942-C-T

46368524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87123950-A-G

46368698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87124089-T-C

http://identifiers.org/hco/2/GRCh38#46368896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87124241-C-A

46369218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87124525-G-A

46369235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87124542-C-G

46369269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87124576-T-G

46369272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87124579-G-C

46369272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87124579-G-T

46369293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87124599-C-T

46369426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87124703-C-T

http://identifiers.org/hco/2/GRCh38#46369468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87124744-C-A

46369519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87124807-G-A

46369594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87124833-C-T

46369635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87124874-T-G

http://identifiers.org/hco/2/GRCh38#46369764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87125720-C-A

46369764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87125720-C-T

46369768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87125724-A-G

http://identifiers.org/hco/2/GRCh38#46369869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87125825-C-A

46369976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87125918-G-A

46370224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87126116-C-T

46370325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87126177-A-G

46370688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87126478-A-G

46370732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87126516-G-A

46371197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87126939-G-C

46371202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87126944-A-G

46371340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87127078-T-C

46371340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87127078-T-G

46371617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87127348-G-A

46371685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87127417-A-G

46371686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87127418-G-T

46371758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87127482-G-T

46371878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87127577-G-A

46371965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87127631-G-A

46372033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87127693-A-G

46372164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87127875-G-C

46372174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87127885-A-G

46372184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87127895-C-T

46372566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87128157-G-A

46372714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87128289-T-C

46372793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87128368-A-T

46372821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87128396-G-A

46372821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87128396-G-C

46373236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87128828-T-C

46373508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129075-T-C

46373587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129132-T-C

46373652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129187-G-A

46373675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129211-G-T

46373732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129292-G-A

46373820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129373-C-G

46373820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129373-C-T

http://identifiers.org/hco/2/GRCh38#46373846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87129407-C-A

46373865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129426-T-C

46373947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129509-G-C

http://identifiers.org/hco/2/GRCh38#46374050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87129590-A-C

46374086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129625-T-C

46374119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129658-G-A

http://identifiers.org/hco/2/GRCh38#46374172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87129712-A-C

46374185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129724-A-T

46374262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129796-C-T

46374263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129797-G-A

46374361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129892-G-A

46374412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87129937-A-G

46374691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87130147-G-C

46374825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87130308-G-T

46374972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87130433-G-C

46375072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87130504-C-T

46375494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87130916-T-A

46375494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87130916-T-C

http://identifiers.org/hco/2/GRCh38#46375540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87130958-C-A

46375540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87130958-C-T

46375556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87130974-G-A

46375556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87130974-G-C

46375556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87130974-G-T

46375574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87130989-G-A

46375574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87130989-G-T

http://identifiers.org/hco/2/GRCh38#46375603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87131031-A-C

http://identifiers.org/hco/2/GRCh38#46375611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87131035-C-A

46375611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: 87131035-C-T

http://identifiers.org/hco/2/GRCh38#46375632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87131053-C-A

46375736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87131154-A-G

46375775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87131193-G-A

http://identifiers.org/hco/2/GRCh38#46375793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87131211-C-A

http://identifiers.org/hco/2/GRCh38#46375936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87131285-C-A

46375936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131285-C-G

46375936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131285-C-T

http://identifiers.org/hco/2/GRCh38#46375939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87131288-C-A

46375939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131288-C-T

46375947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131296-G-A

46375954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131303-C-T

46375970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131320-A-G

46376007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131357-T-A

46376030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131381-G-T

46376285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131615-T-C

46376387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131700-T-C

46376459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131748-T-C

46376459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131748-T-G

http://identifiers.org/hco/2/GRCh38#46376470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87131759-A-C

46376470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131759-A-G

46376470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131759-A-T

46376507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131804-G-A

46376507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131804-G-T

46376520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131817-G-T

46376524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131821-T-A

46376524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87131821-T-C

46376581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87131877-T-C

46376644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87131940-G-A

46376644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87131940-G-T

46376689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87131985-G-C

46376757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132053-G-A

46376795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132092-G-T

46376802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132099-G-A

46376802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132099-G-C

46376824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132121-G-C

46376824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132121-G-T

http://identifiers.org/hco/2/GRCh38#46376853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87132149-A-C

http://identifiers.org/hco/2/GRCh38#46376871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87132160-C-A

46376871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132160-C-T

http://identifiers.org/hco/2/GRCh38#46376903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87132191-C-A

46376903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132191-C-T

46377154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132355-C-T

46377374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132535-C-T

46377705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132848-C-G

46377710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132853-T-C

46377710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132853-T-G

46377714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132857-C-T

46377743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132871-T-C

46377778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132905-C-T

46377782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132909-G-A

46377819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132935-G-A

46377829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132944-C-T

46377839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132954-T-C

46377844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132959-G-A

46377848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132963-G-C

http://identifiers.org/hco/2/GRCh38#46377850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87132965-C-A

46377855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132970-G-A

46377855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87132970-G-T

http://identifiers.org/hco/2/GRCh38#46377907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87133021-C-A

46377907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87133021-C-G

46377907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87133021-C-T

46377946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87133060-G-A

46377946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87133060-G-T

http://identifiers.org/hco/2/GRCh38#46377960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87133074-C-A

46377960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87133074-C-G

46377960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87133074-C-T

46377997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87133111-T-A

http://identifiers.org/hco/2/GRCh38#46378032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87133146-C-A

46378032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87133146-C-T

http://identifiers.org/hco/2/GRCh38#46378048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87133162-C-A

46378048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87133162-C-T

46378110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133222-G-A

46378110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133222-G-T

46378162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133275-A-G

46378184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133296-C-T

46378229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133337-A-G

http://identifiers.org/hco/2/GRCh38#46378231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87133339-C-A

46378231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133339-C-G

46378295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133394-T-C

46378383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133467-C-T

46378432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133531-A-G

http://identifiers.org/hco/2/GRCh38#46378513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87133802-A-C

46378513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133802-A-G

46378513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133802-A-T

46378551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133837-G-A

46378574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133852-A-T

46378593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133871-G-T

http://identifiers.org/hco/2/GRCh38#46378594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87133872-C-A

46378594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87133872-C-T

46378650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87133926-C-T

46378692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87133968-T-C

46378744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense variant
orthologous variants: 87134020-G-A

46380183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87134879-C-T

46380187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87134883-C-T

http://identifiers.org/hco/2/GRCh38#46380301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87134994-C-A

46380301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87134994-C-T

46380405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87135098-C-G

46380405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87135098-C-T

http://identifiers.org/hco/2/GRCh38#46380412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87135105-C-A

46380412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87135105-C-G

46380412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87135105-C-T

46380439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87135132-G-C

46380439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87135132-G-T

46380469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87135162-C-G

46380469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87135162-C-T

http://identifiers.org/hco/2/GRCh38#46380508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87135201-A-C

46380508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87135201-A-G

46380508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87135201-A-T

46380511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87135204-C-G

46380511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87135204-C-T

46380568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87135261-G-A

46380614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87135307-G-A

46380672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87135380-T-G

46380738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87135446-T-G

46380772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87135491-A-G

46380785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87135508-G-T

46380795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87135518-G-A

http://identifiers.org/hco/2/GRCh38#46380836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87135572-A-C

46380840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87135576-C-T

46380923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87135606-A-G

46381097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87135698-G-A

46381097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87135698-G-T

46381120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87135705-T-C

http://identifiers.org/hco/2/GRCh38#46381125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87135710-C-A

46381125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87135710-C-T

http://identifiers.org/hco/2/GRCh38#46381153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87135738-A-C

46381153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87135738-A-T

46381313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87135837-G-T

http://identifiers.org/hco/2/GRCh38#46381337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87135859-C-A

46381463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87136000-G-A

46381547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87136063-G-A

46381781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87136273-G-A

http://identifiers.org/hco/2/GRCh38#46381884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87136358-C-A

46381884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87136358-C-T

http://identifiers.org/hco/2/GRCh38#46381907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87136368-A-C

http://identifiers.org/hco/2/GRCh38#46381941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87136384-A-C

46381941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87136384-A-G

46382149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87136573-G-A

46382149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87136573-G-C

46382149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87136573-G-T

46382444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87136757-C-T

46382506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87136819-G-T

http://identifiers.org/hco/2/GRCh38#46382537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87136850-C-A

46382537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87136850-C-T

46384698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87138567-C-G

46384698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87138567-C-T

http://identifiers.org/hco/2/GRCh38#46384736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87138609-C-A

http://identifiers.org/hco/2/GRCh38#46384767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87138640-C-A

46384767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87138640-C-G

46384767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87138640-C-T

http://identifiers.org/hco/2/GRCh38#46384843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87138716-C-A

46384850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87138723-T-A

46384850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87138723-T-C

46384922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87138813-A-G

46385101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87138965-G-T

46385224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139327-A-T

46385291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139403-C-T

http://identifiers.org/hco/2/GRCh38#46385588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87139729-C-A

46385615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139755-G-A

46385633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139773-T-C

46385688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139828-T-C

46385692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139832-T-C

46385740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139890-G-A

46385740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139890-G-T

46385747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139893-G-C

46385748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139894-G-A

46385748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139894-G-C

46385748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139894-G-T

46385765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139908-T-A

46385765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139908-T-C

46385807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87139950-G-A

http://identifiers.org/hco/2/GRCh38#46385859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87140000-C-A

46385985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87140093-A-G

46386054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87140167-G-A

46386054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87140167-G-T

46386519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87140657-T-C

46386519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87140657-T-G

46386551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87140692-A-G

46386603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3374
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87140744-G-A