http://identifiers.org/hco/1/GRCh38#16018894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141148181-C-A

16018894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141148181-C-T

16018957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141148119-G-A

http://identifiers.org/hco/1/GRCh38#16019096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141148041-C-A

16019096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141148041-C-G

16019096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141148041-C-T

16019099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141148038-T-C

16019124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141148013-T-A

16019124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141148013-T-C

16019124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141148013-T-G

http://identifiers.org/hco/1/GRCh38#16019133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141148007-C-A

16019133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 141148007-C-G

http://identifiers.org/hco/1/GRCh38#16019219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141147941-C-A

16019219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141147941-C-T

http://identifiers.org/hco/1/GRCh38#16019222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141147938-C-A

16019300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141147866-A-G

16019465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141147745-C-T

16019496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141147712-A-G

16019498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141147710-T-C

16019535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141147688-A-G

16019582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141147674-T-G

16019614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147649-G-T

16019624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147639-G-A

16019624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147639-G-T

16019626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147637-G-A

16019626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147637-G-C

16019626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147637-G-T

16019632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147631-G-A

16019632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147631-G-C

16019632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147631-G-T

16019636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147627-G-A

16019636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147627-G-T

http://identifiers.org/hco/1/GRCh38#16019662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141147600-C-A

16019681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147585-C-G

16019681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147585-C-T

http://identifiers.org/hco/1/GRCh38#16019683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141147583-C-A

16019683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147583-C-G

16019683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147583-C-T

16019685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147581-T-G

http://identifiers.org/hco/1/GRCh38#16019701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141147565-A-C

16019701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147565-A-G

http://identifiers.org/hco/1/GRCh38#16019702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141147564-C-A

16019702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147564-C-T

http://identifiers.org/hco/1/GRCh38#16019910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141147356-C-A

http://identifiers.org/hco/1/GRCh38#16019948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141147320-A-C

16019948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141147320-A-G

http://identifiers.org/hco/1/GRCh38#16020017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141147253-C-A

16020038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 141147221-C-G

16020067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: non coding transcript exon variant
orthologous variants: 141147192-T-C

http://identifiers.org/hco/1/GRCh38#16021305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141143988-C-A

16021363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: non coding transcript exon variant
orthologous variants: 141143931-C-T

16021422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: non coding transcript exon variant
orthologous variants: 141143818-A-G

http://identifiers.org/hco/1/GRCh38#16021586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141143699-C-A

16021586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143699-C-T

http://identifiers.org/hco/1/GRCh38#16021597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141143687-C-A

http://identifiers.org/hco/1/GRCh38#16021626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141143662-C-A

http://identifiers.org/hco/1/GRCh38#16021628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141143660-C-A

16021628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141143660-C-T

16021644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141143644-T-C

16021661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141143626-T-C

16021700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141143590-G-A

http://identifiers.org/hco/1/GRCh38#16021709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141143581-C-A

16021709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141143581-C-G

16021709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141143581-C-T

http://identifiers.org/hco/1/GRCh38#16021720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141143571-C-A

16021720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141143571-C-G

16021720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141143571-C-T

16021721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141143570-T-C

http://identifiers.org/hco/1/GRCh38#16021757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141143534-C-A

16021757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143534-C-G

16021757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143534-C-T

16021763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143528-G-A

16021763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143528-G-T

16021812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143477-A-G

16021820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143469-G-A

16021820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143469-G-T

http://identifiers.org/hco/1/GRCh38#16021995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141143326-A-C

16022000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141143321-A-G

16022090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143220-A-G

16022090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143220-A-T

16022092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143218-T-A

16022092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143218-T-C

16022092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143218-T-G

http://identifiers.org/hco/1/GRCh38#16022117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141143180-C-A

16022117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143180-C-T

16022135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143162-A-G

16022135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143162-A-T

http://identifiers.org/hco/1/GRCh38#16022140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141143157-C-A

16022140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143157-C-T

16022160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143147-T-C

16022160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143147-T-G

http://identifiers.org/hco/1/GRCh38#16022174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141143135-C-A

http://identifiers.org/hco/1/GRCh38#16022195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141143111-C-A

16022242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143080-A-G

16022300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141143035-G-A

16022374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142936-T-C

http://identifiers.org/hco/1/GRCh38#16022497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141142733-C-A

16022497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142733-C-G

16022497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142733-C-T

16022558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142661-A-G

16022574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142645-G-A

16022574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142645-G-T

http://identifiers.org/hco/1/GRCh38#16022698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141142526-C-A

16022698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141142526-C-G

16022698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141142526-C-T

16022730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142494-G-A

16022730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142494-G-C

16022730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142494-G-T

http://identifiers.org/hco/1/GRCh38#16022733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141142491-C-A

16022733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142491-C-T

16022735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142489-T-C

http://identifiers.org/hco/1/GRCh38#16022740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141142484-C-A

16022740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142484-C-T

16022751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142473-G-A

16022751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142473-G-T

http://identifiers.org/hco/1/GRCh38#16022813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141142425-C-A

16022813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142425-C-G

http://identifiers.org/hco/1/GRCh38#16022827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141142407-C-A

16022827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142407-C-G

16022827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142407-C-T

16022835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142399-T-A

16022864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142381-G-A

16022864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142381-G-T

16022865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142380-A-G

16022865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142380-A-T

16022878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142369-G-C

16023206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142252-T-A

16023378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141142156-C-T

http://identifiers.org/hco/1/GRCh38#16023418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141142123-A-C

http://identifiers.org/hco/1/GRCh38#16023794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141141887-C-A

16023794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 141141887-C-T

16023883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 141141799-C-T

http://identifiers.org/hco/1/GRCh38#16023944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141141738-C-A

16023944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141738-C-G

16023944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141738-C-T

http://identifiers.org/hco/1/GRCh38#16023977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141141702-C-A

16023977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141702-C-T

16023983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141698-G-A

16023983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141698-G-T

16023991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141690-C-T

http://identifiers.org/hco/1/GRCh38#16024003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141141678-C-A

16024003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141678-C-G

http://identifiers.org/hco/1/GRCh38#16024005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141141676-A-C

http://identifiers.org/hco/1/GRCh38#16024050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141141634-C-A

16024050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141634-C-T

16024682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141398-G-T

16024787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141141298-T-C

16024822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141141263-A-G

16024822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141141263-A-T

16024823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141141262-C-T

16024876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141141209-A-T

16024913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141142-C-G

16024971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141085-G-A

16024971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141085-G-C

16024974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141082-G-A

16024974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141082-G-C

16024974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141082-G-T

16024978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141078-C-T

16025036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141141008-A-T

16025060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141140987-C-T

16025227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141123472-G-A

16025227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141123472-G-C

16025232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141123467-C-G

16025861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141139830-T-C

16026006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141139723-G-A

16026006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141139723-G-C

16026006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141139723-G-T

16026010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141139719-T-A

16026010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141139719-T-C

16026031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141139699-G-A

16026031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141139699-G-T

16026067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141139680-T-G

16026531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 141139134-T-C

16026640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141139021-G-A

16026640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141139021-G-T

16026724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141138950-G-T

16026797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122246-G-A

16026833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122197-T-A

16026841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141122189-C-T

http://identifiers.org/hco/1/GRCh38#16026899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141122147-C-A

16026899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122147-C-G

16026899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122147-C-T

16026908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 141122138-G-A

http://identifiers.org/hco/1/GRCh38#16026920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141122126-C-A

16026920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122126-C-G

16026920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122126-C-T

http://identifiers.org/hco/1/GRCh38#16026922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141122124-C-A

16026922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122124-C-G

16026922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122124-C-T

16026953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122113-G-C

16026953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122113-G-T

16026993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122082-T-A

16026993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122082-T-C

16026993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122082-T-G

http://identifiers.org/hco/1/GRCh38#16026999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141122076-A-C

16026999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122076-A-G

16026999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122076-A-T

16027039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122040-A-G

16027039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122040-A-T

16027062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141122015-A-G

16027150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141121934-C-G

16027150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141121934-C-T

16027260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141138857-C-T

16027279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141138846-G-A

16027414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141138713-G-A

16027460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141138666-C-G

16027498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141138640-T-C

http://identifiers.org/hco/1/GRCh38#16027503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141138635-C-A

16027503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141138635-C-T

16027592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141120322-G-C

16027592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141120322-G-T

16027748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141138156-G-A

16027748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141138156-G-C

http://identifiers.org/hco/1/GRCh38#16027797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141138115-C-A

16027797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141138115-C-T

http://identifiers.org/hco/1/GRCh38#16027811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141138097-C-A

16027811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141138097-C-T

16028211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141137742-G-A

http://identifiers.org/hco/1/GRCh38#16028214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141137739-C-A

16028214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141137739-C-T

16028232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141137721-G-T

16028247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141137706-A-G

http://identifiers.org/hco/1/GRCh38#16028253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141137702-C-A

16028253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141137702-C-T

16028361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141137630-C-T

http://identifiers.org/hco/1/GRCh38#16028473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141137548-C-A

16028473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141137548-C-G

16028473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141137548-C-T

16028483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141137543-T-C

http://identifiers.org/hco/1/GRCh38#16028493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141137533-C-A

16028493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141137533-C-G

16028493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141137533-C-T

http://identifiers.org/hco/1/GRCh38#16028543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141137473-C-A

16028543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141137473-C-G

16028543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141137473-C-T

16028646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141137315-T-G

http://identifiers.org/hco/1/GRCh38#16028960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141136951-C-A

16028960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136951-C-T

16028968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136943-A-T

16028986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136925-G-T

16029012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136899-C-T

http://identifiers.org/hco/1/GRCh38#16029016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141136895-C-A

16029112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136822-C-T

http://identifiers.org/hco/1/GRCh38#16029135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141136799-A-C

16029135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 141136799-A-T

16029151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141136783-C-T

16029209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 141136725-C-G

16029209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 141136725-C-T

16029210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141136724-G-A

16029210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 141136724-G-T

16029249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141136685-C-T

16029276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141136658-C-G

16029276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141136658-C-T

16029356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136350-G-C

16029361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136345-G-A

16029361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136345-G-C

16029361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136345-G-T

16029374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136332-C-T

http://identifiers.org/hco/1/GRCh38#16029375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141136331-A-C

16029375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136331-A-G

16029380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136308-G-T

16029438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136251-T-C

16029441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136248-T-C

16029559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136112-G-T

http://identifiers.org/hco/1/GRCh38#16029602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141136065-C-A

16029602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136065-C-G

16029602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136065-C-T

http://identifiers.org/hco/1/GRCh38#16029624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141136043-C-A

16029624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136043-C-T

16029650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141136020-C-T

16029828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135857-A-G

16029874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135815-T-C

http://identifiers.org/hco/1/GRCh38#16029949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141135740-C-A

16029949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135740-C-G

16029949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135740-C-T

http://identifiers.org/hco/1/GRCh38#16029973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141135717-A-C

16029973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141135717-A-G

16029973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141135717-A-T

16030120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135596-G-A

16030120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135596-G-T

16030147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135588-G-T

16030148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135587-T-A

16030148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135587-T-C

16030148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135587-T-G

16030176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135581-T-C

16030176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135581-T-G

16030241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135533-C-T

16030325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135461-T-G

http://identifiers.org/hco/1/GRCh38#16030337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141135452-C-A

16030337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135452-C-G

16030363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135423-A-G

http://identifiers.org/hco/1/GRCh38#16030371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141135415-C-A

16030475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141135312-T-G

16030481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141135306-G-A

16030535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141135252-A-T

16030570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 141135217-G-A

http://identifiers.org/hco/1/GRCh38#16030577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141135210-A-C

16030649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141135138-C-G

16030728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135070-G-C

16030728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135070-G-T

http://identifiers.org/hco/1/GRCh38#16030762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141135040-C-A

16030762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135040-C-G

16030762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135040-C-T

16030786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135017-G-A

16030786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135017-G-T

16030787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135016-G-A

16030787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141135016-G-T

http://identifiers.org/hco/1/GRCh38#16030817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141134987-C-A

16031026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141134883-C-G

16031026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141134883-C-T

16031036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141134873-C-T

16031146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141134783-A-T

16031720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141134521-G-A

16031727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141134514-T-A

16031796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141134445-T-C

16031913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141134300-G-A

16031913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141134300-G-T

16032047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141134144-C-T

16032149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141134068-T-C

http://identifiers.org/hco/1/GRCh38#16032173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141134037-C-A

http://identifiers.org/hco/1/GRCh38#16032177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141134033-C-A

16032177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141134033-C-G

http://identifiers.org/hco/1/GRCh38#16032180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141134030-C-A

16032180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141134030-C-T

http://identifiers.org/hco/1/GRCh38#16032192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141134018-C-A

16032192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141134018-C-T

16032361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141132525-C-T

16032445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_acceptor_variant, splice_region_variant
orthologous variants: 141132442-G-T

http://identifiers.org/hco/1/GRCh38#16032477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141132410-C-A

http://identifiers.org/hco/1/GRCh38#16032505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141132382-C-A

16032576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141114362-G-A

16032583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141114355-T-G

16032715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141113843-G-C

16032747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141113810-G-A

16032945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141112852-G-A

16032946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141112851-G-T

16032982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141132279-G-A

16032982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141132279-G-T

http://identifiers.org/hco/1/GRCh38#16033022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141132240-C-A

16033022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141132240-C-G

16033022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141132240-C-T

http://identifiers.org/hco/1/GRCh38#16033036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141132226-C-A

16033036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141132226-C-T

16033101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141132200-G-A

http://identifiers.org/hco/1/GRCh38#16033159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141132158-C-A

16033159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141132158-C-T

http://identifiers.org/hco/1/GRCh38#16033215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141132103-A-C

16033238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 141132080-C-T

16033242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141132076-G-A

16033277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141132041-G-T

16033287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141112557-G-A

http://identifiers.org/hco/1/GRCh38#16033293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141112556-C-A

16033306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141112543-G-T

16033364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141112480-A-G

16033364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141112480-A-T

16033365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141112479-T-C

16033365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141112479-T-G

16033462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141112412-T-C

16033524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141112333-T-C

16033524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141112333-T-G

16033525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141112332-G-A

16033525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141112332-G-C

16033525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141112332-G-T

16033536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141132027-G-A

16033536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141132027-G-T

16033559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141131999-T-A

16033559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141131999-T-C

16033559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141131999-T-G

http://identifiers.org/hco/1/GRCh38#16033571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141131982-C-A

16033571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141131982-C-G

16033571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141131982-C-T

16033644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141131908-C-G

16033667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141131885-A-T

16033683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141131866-G-A

http://identifiers.org/hco/1/GRCh38#16033692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141131850-C-A

16033692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141131850-C-G

16033692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141131850-C-T

16033772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141112107-T-G

16033773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141112106-T-A

http://identifiers.org/hco/1/GRCh38#16033774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141112105-C-A

16033774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141112105-C-G

16033812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141112070-G-T

16033825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141112046-T-A

16033825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141112046-T-C

16033825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141112046-T-G

16033868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141112002-C-T

16033872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141111998-G-A

16033872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141111998-G-T

http://identifiers.org/hco/1/GRCh38#16033945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141111997-A-C

16033945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141111997-A-G

http://identifiers.org/hco/1/GRCh38#16033949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141111993-C-A

16033949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141111993-C-G

16033949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141111993-C-T

http://identifiers.org/hco/1/GRCh38#16033953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141111989-A-C

16033953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141111989-A-G

16033953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141111989-A-T

http://identifiers.org/hco/1/GRCh38#16034011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141111963-C-A

16034011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141111963-C-G

16034011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141111963-C-T

16034015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141111959-G-A

16034015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141111959-G-C