66016857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19552432-G-A

http://identifiers.org/hco/8/GRCh38#66019132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19557029-A-C

66019215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19557108-T-G

66019262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19557143-C-G

http://identifiers.org/hco/8/GRCh38#66019366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19557241-C-A

66019373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19557248-T-C

66020577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19560946-G-A

66021166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 19561172-A-G

66021174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19561180-T-C

66021351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19562612-C-T

66021483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron variant
orthologous variants: 19562712-A-G

66021558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19562786-G-T

66022098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19563364-T-A

66022122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19563388-T-C

http://identifiers.org/hco/8/GRCh38#66022192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19563455-C-A

66022219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19563486-G-A

66022240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19563506-G-A

66022425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19563683-G-T

66022555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19563803-A-G

66022801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19564151-C-T

66022888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19564234-C-T

66022979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19564325-C-T

66023351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19564651-A-T

66023400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19564703-A-G

66023835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19565490-G-A

66023861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19565511-T-C

66023897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19565547-G-T

66023904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19565554-C-G

66023935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19565583-T-G

66026474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19566183-A-G

66026651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19566361-G-A

66026708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19566418-G-A

66026781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19566489-G-C

http://identifiers.org/hco/8/GRCh38#66026882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#19566591-C-A

66026882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19566591-C-T

66026890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19566599-T-G

66027048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19566639-C-T

66027130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19566702-C-T

http://identifiers.org/hco/8/GRCh38#66027230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19566795-C-A

66027230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19566795-C-T

66027231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19566796-G-A

66027430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19566963-G-T

66027605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19567135-G-A

66027723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19567265-G-A

66027780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19567312-T-C

66027781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19567313-C-T

66027897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19567412-G-A

66027950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19567463-G-A

66028137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19567631-C-T

66028199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19567686-A-G

66028288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19567760-G-A

66028317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19567775-G-A

http://identifiers.org/hco/8/GRCh38#66028400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19567853-C-A

66028409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19567862-G-A

66028409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19567862-G-C

66028513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19567966-C-T

66028555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19568007-C-T

66028744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19568162-G-A

http://identifiers.org/hco/8/GRCh38#66028787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19568184-A-C

http://identifiers.org/hco/8/GRCh38#66028796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19568193-C-A

66028921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19568307-C-T

66029103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19568461-C-T

66029136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19568473-G-C

66029148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19568485-C-T

66029193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19568514-A-T

66029255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19568575-G-A

66029491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19568772-T-C

66029656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19568932-A-G

66029663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19568939-G-A

66029792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19569042-C-G

66029818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19569066-T-A

66029818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19569066-T-C

66029840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19569088-C-T

66030966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19572920-T-G

66031150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19573094-G-A

66031721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19573555-T-C

66031951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19573718-T-G

66032006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19573757-G-A

66032053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19573804-T-C

http://identifiers.org/hco/8/GRCh38#66032151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19573899-A-C

66032485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19574192-C-T

66032523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19574230-G-A

66032527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19574234-C-G

66032879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19574537-A-G

66032880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19574538-A-G

66032964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19574620-C-T

66032994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19574650-C-T

66033047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19574704-C-T

66033107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19574753-G-T

66033372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575015-G-A

66033547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575193-A-G

66033650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575300-C-T

66033820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575441-A-T

66033933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575533-C-T

66033949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575546-G-T

66034035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575617-C-T

66034220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575739-A-G

66034220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575739-A-T

66034331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575844-G-A

66034362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575868-C-T

66034433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575930-C-T

66034537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19576036-T-A

66034541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19576040-C-G

66034621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19576132-G-A

66036631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19576475-T-C

66036666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19576510-T-C

66036878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19576815-G-A

66036891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19576853-G-C

66036894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19576856-A-T

66037447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19577460-G-A

66037504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19577509-C-G

66037803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19577734-G-A

66037936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19577780-T-G

66038039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19577886-G-A

66038339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578137-C-T

66038363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578161-G-T

66038541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578310-C-T

66038852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578516-G-A

66038852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578516-G-C

66038853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578517-G-T

66039163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578734-G-A

66039772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19579931-G-C

66040585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19580874-T-C

66040585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19580874-T-G

66040611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19580897-T-G

66040649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19580934-G-A

66040823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19581092-T-C

66040925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19581200-A-G

66041040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19581399-G-C

66041138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19581497-T-C

http://identifiers.org/hco/8/GRCh38#66041368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19582753-C-A

66041609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19583638-T-C

66041774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19583762-C-T

66042073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19584109-C-G

66042073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19584109-C-T

66042102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19584138-T-C

66042103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19584139-T-C

66042214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19584243-G-T

66042342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19584409-T-C

66042733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19584657-T-C

66042765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19584666-T-C

66043247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19585082-A-G

66043325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19585147-G-C

66043354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19585174-T-C

http://identifiers.org/hco/8/GRCh38#66043364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19585183-C-A

66044164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19585662-A-T

66044450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19585910-A-G

http://identifiers.org/hco/8/GRCh38#66044532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19585979-C-A

66044592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19586037-G-T

66044921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19586365-A-G

66044946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19586390-C-T

66045170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19586582-T-C

66045467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19586856-T-C

66045511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19586891-C-G

http://identifiers.org/hco/8/GRCh38#66045552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19586928-C-A

66045552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19586928-C-T

66045619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19586986-C-T

66045734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19587089-A-T

66045866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19587221-T-C

66045875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19587230-G-T

66045953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19587314-A-G

66046069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19587456-C-T

66046150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19587506-T-C

66046451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19587761-G-C

66046451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19587761-G-T

http://identifiers.org/hco/8/GRCh38#66046602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19587897-C-A

66046641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19587930-A-G

http://identifiers.org/hco/8/GRCh38#66046655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19587971-C-A

66046655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19587971-C-T

66046684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19588003-C-T

66046709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19588023-T-C

66046798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19588104-A-G

66046815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19588121-A-T

http://identifiers.org/hco/8/GRCh38#66046960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19588266-C-A

http://identifiers.org/hco/8/GRCh38#66047094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19588348-C-A

66047094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19588348-C-G

66047127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19588380-G-C

66047202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19588477-G-A

66047457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19589105-A-T

http://identifiers.org/hco/8/GRCh38#66047604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19589219-A-C

66047832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19589415-T-A

66048089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19589644-T-C

66048151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19589686-C-T

66048356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19589857-C-G

66048356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19589857-C-T

66048363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19589864-G-A

http://identifiers.org/hco/8/GRCh38#66049731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19590775-C-A

66050269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19591752-G-A

66050400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19591875-C-T

66050650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19592143-G-T

66050709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19592204-A-G

66050749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19592243-A-G

66050870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19592357-T-C

66051367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19600729-G-A

66051788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19601152-T-G

66051934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19601302-A-G

http://identifiers.org/hco/8/GRCh38#66053955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19601666-C-A

66053955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19601666-C-T

66054003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19601712-T-G

66054330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19602010-T-C

http://identifiers.org/hco/8/GRCh38#66054351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19602031-A-C

66054363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19602043-A-T

66054464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19602145-G-T

66054630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19602295-G-T

66054733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19602385-C-T

66055398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19603015-G-A

66055494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19603152-A-G

66055618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19603246-C-T

http://identifiers.org/hco/8/GRCh38#66055679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19603306-C-A

http://identifiers.org/hco/8/GRCh38#66056146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19603787-C-A

66056146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19603787-C-T

66056192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19603842-C-T

66056556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19604129-A-G

66056717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19604294-T-A

66056717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19604294-T-C

66056782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19604340-G-A

66056789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19604347-A-G

66056837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19604395-G-T

66056933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19604430-G-T

66056936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19604433-T-C

http://identifiers.org/hco/8/GRCh38#66057206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19604460-C-A

66057305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19604545-C-G

http://identifiers.org/hco/8/GRCh38#66057340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19604578-C-A

66057382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19604628-T-A

66057382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19604628-T-G

http://identifiers.org/hco/8/GRCh38#66057492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19604737-C-A

http://identifiers.org/hco/8/GRCh38#66057590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19604830-C-A

66057590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19604830-C-T

66057799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605025-T-C

66058328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19606484-C-T

66058553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19606703-G-A

66058553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19606703-G-T

66058661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19606813-C-T

66058672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19606824-C-T

66058802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19606944-C-T

66058827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19606973-G-C

66058963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19607092-G-A

http://identifiers.org/hco/8/GRCh38#66059229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19607360-C-A

66059229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19607360-C-T

66059253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19607381-A-G

66059340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19607462-T-A

66059483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19607592-T-C

66059530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19607638-T-C

66059698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19608125-G-C

66059999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19608424-G-A

66060262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19608574-C-T

66060459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19608729-C-T

66061714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19608963-A-T

66062035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19609258-C-T

http://identifiers.org/hco/8/GRCh38#66062043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19609266-A-C

66062133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19609344-C-T

http://identifiers.org/hco/8/GRCh38#66062278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19609501-A-C

66062967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19610180-A-T

66063604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19610775-C-T

66063624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19610795-C-T

http://identifiers.org/hco/8/GRCh38#66063721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19610878-A-C

66063721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19610878-A-G

66064675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19615918-A-G

66064866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19616526-T-A

66064884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19616543-T-C

66065378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19617028-T-C

66065457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19617107-A-G

66065573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19617200-C-T

66065588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19617215-T-C

66065603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19617231-T-C

66065670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19617291-A-T

http://identifiers.org/hco/8/GRCh38#66065678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19617297-A-C

66065678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19617297-A-T

66065721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19617327-G-A

66065731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19617336-G-A

66067236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19617912-G-A

66067236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19617912-G-C

66067249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19617925-C-T

http://identifiers.org/hco/8/GRCh38#66067266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19617937-A-C

66067414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19618203-G-A

66067414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19618203-G-T

66067469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19618252-A-G

66067864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19618639-C-T

66068083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19618799-A-G

66074552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19620859-A-G

66074593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19620900-T-C

66075356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19621457-C-T

66075665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19623128-A-T

66076023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19628225-G-A

66076235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19628452-A-G

http://identifiers.org/hco/8/GRCh38#66076322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19628526-C-A

66076455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19628642-G-T

66076563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19628729-T-C

66076571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19628737-A-T

66076648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19628813-T-C

http://identifiers.org/hco/8/GRCh38#66076650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19628817-A-C

66076650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19628817-A-G

66076650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19628817-A-T

66076738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19628905-C-G

66076738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 19628905-C-T

66076892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19629058-T-C

http://identifiers.org/hco/8/GRCh38#66076897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19629067-A-C

66076897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19629067-A-G

http://identifiers.org/hco/8/GRCh38#66076926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19629097-C-A

66076926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19629097-C-T

66076993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19629164-A-G

66076993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19629164-A-T

66077537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19629686-G-A

66077669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19629810-T-A

66077800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19630846-A-G

66077815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19630859-C-T

http://identifiers.org/hco/8/GRCh38#66078173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19631175-A-C

66078328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19631321-C-G

66078727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19631667-C-T

66078728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19631668-G-A

66078863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19631799-G-A

66079384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19632278-A-G

66079684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19632514-G-A

66079851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19632624-A-G

66079897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19632668-T-C

66080005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19632759-G-C

66080121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19632860-C-T

66080193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19632930-T-C

66080258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19632997-G-T

66080265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19633004-A-G

66080363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19633097-C-G

66080363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19633097-C-T

66080553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19633288-G-A

66080563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19633298-G-C

66080563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19633298-G-T

66080588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19633319-A-G

66080803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19633515-A-G

http://identifiers.org/hco/8/GRCh38#66080836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19633550-A-C

66081271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19633896-G-C

http://identifiers.org/hco/8/GRCh38#66081337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19633956-A-C

66081337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19633956-A-G

66081337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19633956-A-T

66081357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19633975-C-G

66081357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19633975-C-T

66081384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19633998-A-G

66081602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19634184-T-A

66081609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19634191-T-C

66081659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19634243-G-T

66081826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19634422-T-G

66081993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19634588-T-C

http://identifiers.org/hco/8/GRCh38#66082044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19634619-C-A

66082048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19634623-C-G

66082053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19634628-G-A

66082080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19634655-A-G

66082351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19636150-A-G

66082402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19636177-G-T

66082443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19636217-G-A

66082504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19636278-C-T

66082806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19636552-G-T

66082876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19636627-C-T

66083508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19636864-A-G

66083687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19637045-T-C

66083832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19637161-G-C

66083932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19637244-G-T

66083966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19637253-G-A

66084035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19637331-A-G

66084133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19637425-C-T

66086761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19637691-C-G

66086959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19637883-C-T

66089637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19659501-A-G

66089745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19659606-G-A

66089881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19659713-A-G

66089905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19659730-A-G

66089990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19659812-G-C

66089990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19659812-G-T

66090003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19659825-C-T

66090359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19659952-G-C

66090547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19660129-C-T

66090689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19660231-G-C

66090702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19660243-G-A

66090703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19660244-G-A

66091320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19660963-T-G

66091325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19660968-G-C

66091657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19661289-C-G

66091657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19661289-C-T

66091803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19661417-G-A

66091931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19661504-A-G

66099431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19664372-T-C

66099444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19664385-T-A

http://identifiers.org/hco/8/GRCh38#66099449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19664390-C-A

66099459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19664400-T-G

66099744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19664569-A-G

http://identifiers.org/hco/8/GRCh38#66099827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19664602-A-C

http://identifiers.org/hco/8/GRCh38#66099854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19664620-C-A

66099854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19664620-C-T

66100041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 19664812-C-T

66100049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 19664820-G-A

66100049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 19664820-G-T

66100193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 19664956-G-A

66100193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 19664956-G-T

66100265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 19665026-T-A

66100274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 19665035-C-G

http://identifiers.org/hco/8/GRCh38#66100351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19665112-C-A

66100351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 19665112-C-T

http://identifiers.org/hco/8/GRCh38#66100401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#19665169-C-A

66100612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24138
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 19665328-A-G