75601727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79974070-G-T

75602122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79974411-G-A

75602122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79974411-G-T

75602135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79974422-G-A

75602135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79974422-G-T

http://identifiers.org/hco/6/GRCh38#75602146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#79974432-C-A

http://identifiers.org/hco/6/GRCh38#75602157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#79974443-C-A

75602157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79974443-C-G

75602157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79974443-C-T

http://identifiers.org/hco/6/GRCh38#75602204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#79974509-C-A

75602204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79974509-C-T

75602248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 79974553-G-A

http://identifiers.org/hco/6/GRCh38#75602372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79974657-C-A

75602372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79974657-C-T

75602390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 79974673-C-T

75602437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79974718-A-G

75602437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79974718-A-T

75602480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 79974761-G-A

75602480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 79974761-G-C

75602480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 79974761-G-T

75602659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79974945-C-G

75602659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79974945-C-T

75602684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79974968-G-A

75602684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79974968-G-T

75602691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79974977-A-G

75602691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79974977-A-T

75602702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79974993-G-A

75602702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79974993-G-C

75602714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79975005-A-G

75602826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79975107-G-T

75603748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79976143-C-T

http://identifiers.org/hco/6/GRCh38#75603831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79976244-C-A

75604115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79976528-A-G

75605868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79978327-A-G

75605955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79978396-G-T

75606236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79978660-C-T

75607812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79981984-C-G

75607821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79981993-A-T

75607855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79982022-G-A

75607855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79982022-G-C

75608895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79983552-T-G

75609019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79983704-A-G

75609224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79983890-C-T

75609245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79983903-C-G

75609245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79983903-C-T

75609357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79984007-G-A

75616123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79987969-T-C

75620710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79994140-A-G

75620878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79994271-A-T

75621028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79994343-T-G

75621091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79994403-C-T

75621197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79994501-G-A

75621495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79994676-A-G

75621620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79994800-T-A

75621620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 79994800-T-C

75621657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79994832-T-C

75621686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79994861-A-G

75621932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79995058-C-T

75622006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79995111-A-G

75622154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79995252-T-C

75622660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79995702-A-T

75622783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79995847-T-G

75622962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79996253-T-A

75623245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79996516-C-G

75623349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79996599-A-G

75623388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79996621-C-T

75623567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79996775-A-G

75623748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79996947-G-A

75623748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79996947-G-T

http://identifiers.org/hco/6/GRCh38#75623751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79996950-C-A

75623751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79996950-C-T

http://identifiers.org/hco/6/GRCh38#75623754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79996953-A-C

75623754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79996953-A-G

75623754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79996953-A-T

75623755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79996999-T-A

75623755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79996999-T-C

75623755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79996999-T-G

http://identifiers.org/hco/6/GRCh38#75623758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79997002-C-A

75623758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79997002-C-T

75623853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79997085-G-A

75623853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79997085-G-T

75633109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79998652-A-G

75633119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79998662-T-C

75633120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79998663-C-G

75633141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79998688-A-G

75633259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79998759-T-A

75633391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79998918-T-A

http://identifiers.org/hco/6/GRCh38#75633434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79998967-A-C

75633434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79998967-A-G

75633538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79999503-A-G

75633787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

75634105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80000347-C-T

75634628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80000704-A-G

75634628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80000704-A-T

75634716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80000828-G-A

75634716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80000828-G-T

http://identifiers.org/hco/6/GRCh38#75634717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80000829-C-A

75634717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 80000829-C-T

75634721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80000833-A-G

75634731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80000843-A-G

75634820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80000931-T-C

75634932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80001026-T-C

75634983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80001078-T-C

75635618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80001681-C-G

http://identifiers.org/hco/6/GRCh38#75635726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80001784-A-C

75635763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80001830-A-G

75635776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80001843-T-A

75636304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80002428-G-C

75636434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80002593-G-A

75636434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80002593-G-T

75638276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80004260-T-C

75638413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80004379-G-A

75638558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80004451-G-T

75638564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80004457-G-T

75638582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80004475-G-A

75638604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80004496-A-G

75638604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80004496-A-T

75638606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80004498-A-G

75638606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80004498-A-T

75638620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80004509-A-T

75638624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80004513-T-A

http://identifiers.org/hco/6/GRCh38#75638661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80004597-C-A

75638661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80004597-C-G

75638661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80004597-C-T

75639075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80004708-C-T

75639546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80005534-C-T

75640542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80006026-G-A

75640542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80006026-G-C

75640607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80006092-A-G

75647616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80010866-T-C

75647714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80010958-A-G

75647715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80010959-T-G

75647766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80011011-T-C

75647780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80011025-T-A

75647785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80011030-T-G

75647788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80011033-G-A

75647788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80011033-G-T

http://identifiers.org/hco/6/GRCh38#75647794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80011039-A-C

75647794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80011039-A-G

75647799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 80011044-T-A

75647855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80011103-A-G

75647969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80011230-C-G

75647969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80011230-C-T

75648569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80012579-C-T

http://identifiers.org/hco/6/GRCh38#75649486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80013371-C-A

75650100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80013711-T-G

75650430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80014031-A-G

75651066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80015074-G-T

75651164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80015191-T-G

75651260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80015289-C-T

75659267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80018598-A-G

75659448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80018874-T-C

75659512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80019092-G-A

75665568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80023008-T-G

75665583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80023022-A-G

75666311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80023175-A-G

75666374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80023230-T-G

75666401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80023257-G-A

75666401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80023257-G-C

75666542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: intron variant
orthologous variants: 80023532-G-A

75666777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: stop gained
orthologous variants: 80023882-C-T

75667022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80024108-T-A

75667022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80024108-T-C

75667022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80024108-T-G

75667211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80024293-T-C

75667243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80024789-C-T

75670447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80025657-G-T

75670454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80025664-T-A

75670753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80025953-T-C

75670872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80026066-T-G

75675397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80028566-G-A

75675397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80028566-G-T

75675400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80028569-A-G

75675454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 80028628-A-G

75675454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 80028628-A-T

75675490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80028663-T-A

75675518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80028686-G-A

75675518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80028686-G-T

75675698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80028819-G-A

75675698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80028819-G-T

75675701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80028822-G-A

75675701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80028822-G-C

75675701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80028822-G-T

75675814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80029095-T-C

75675814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80029095-T-G

75675850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80029136-T-C

75675882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 80029168-G-C

75676029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 80029315-T-C

75676326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80029616-T-A

75676361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80029645-C-T

75677134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80031106-A-G

75677158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80031130-C-T

75677288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80031260-T-A

75677288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80031260-T-C

75677291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80031263-A-G

http://identifiers.org/hco/6/GRCh38#75677859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80031757-C-A

75677859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80031757-C-G

75677859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80031757-C-T

75678594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80033436-A-G

http://identifiers.org/hco/6/GRCh38#75678672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80033514-C-A

http://identifiers.org/hco/6/GRCh38#75678859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80033666-C-A

http://identifiers.org/hco/6/GRCh38#75678944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80033744-C-A

75678947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80033747-A-T

http://identifiers.org/hco/6/GRCh38#75678967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80033765-C-A

75678967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80033765-C-G

75678967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80033765-C-T

http://identifiers.org/hco/6/GRCh38#75679041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80033846-C-A

75679041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80033846-C-T

75679067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80033888-T-C

75693787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80037162-C-T

75693907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80037276-C-T

75695909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80038126-A-G

75696145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80038761-T-A

75696260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80038862-G-A

75696330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80038923-A-G

75696481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80038990-T-G

75696584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80039059-C-T

75697282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80040035-T-C

75697385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80040136-G-C

75697385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80040136-G-T

75697509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80040255-T-A

75697632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80040343-G-A

75697632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80040343-G-T

http://identifiers.org/hco/6/GRCh38#75697663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80040363-C-A

75697740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80040436-C-T

75697777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80040473-A-T

75697786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80040477-G-A

http://identifiers.org/hco/6/GRCh38#75697808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80040502-C-A

75697808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80040502-C-T

75697825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80040515-T-A

75697826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80040516-T-G

http://identifiers.org/hco/6/GRCh38#75697866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80040530-A-C

75697921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80040581-G-T

75697923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80040583-T-G

75697931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80040590-A-G

http://identifiers.org/hco/6/GRCh38#75698024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80040682-A-C

75698024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80040682-A-G

75698077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80040752-C-G

75698077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80040752-C-T

75699375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80041658-G-A

75699375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80041658-G-T

75701496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80043302-A-T

75702529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80043623-T-C

75703060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 80044152-A-G

75706385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80044657-C-G

75706536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80044798-A-T

75706607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80044863-T-G

75706675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80044998-G-A

75706675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80044998-G-C

75706917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80045316-A-G

75706939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80045338-G-A

75709381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80046203-T-G

http://identifiers.org/hco/6/GRCh38#75709456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80046258-A-C

75709477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80046279-G-A

75709477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80046279-G-T

http://identifiers.org/hco/6/GRCh38#75709488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80046290-A-C

75709555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 80046354-T-C

75709579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 80046378-T-C

75709682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80046453-T-G

http://identifiers.org/hco/6/GRCh38#75709690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80046461-C-A

http://identifiers.org/hco/6/GRCh38#75709696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80046467-A-C

75709696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80046467-A-G

75709716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80046472-T-A

75709943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80046549-C-T

75710012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80046633-T-C

75710012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80046633-T-G

75710451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80047159-A-G

75711186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80047957-A-G

75711203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80047969-A-G

75711290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80048054-A-G

75711310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80048076-G-A

75711310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80048076-G-T

75711345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 80048117-T-C

75711434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80048204-A-G

75711452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80048221-T-C

75712079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80048672-T-C

75712715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80048906-G-A

75713417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049278-T-C

75713417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049278-T-G

75713525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 80049377-A-G

75713596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049458-T-A

75713596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049458-T-C

75713628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049486-G-C

75713628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049486-G-T

75713630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049488-A-G

75713638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049496-A-G

75713644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049500-G-A

75713644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049500-G-T

75713765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 80049617-G-T

75713792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 80049644-A-G

75713891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049738-T-A

75713891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049738-T-C

75713983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049799-T-C

75714112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049894-A-G

75714207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80049939-A-G

75714299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80050024-C-T

75714369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80050086-G-C

75714389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80050101-A-G

http://identifiers.org/hco/6/GRCh38#75714404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80050117-A-C

75714404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80050117-A-G

75714404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80050117-A-T

75714425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80050134-C-T

75714489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80050194-A-G

75714927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80050488-G-A

75715084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80050666-C-T

75715093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80050675-A-G

http://identifiers.org/hco/6/GRCh38#75715146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80050723-A-C

75715225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80050793-T-A

http://identifiers.org/hco/6/GRCh38#75715239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80050807-C-A

75715252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80050820-G-A

75715421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 80050968-G-A

http://identifiers.org/hco/6/GRCh38#75715668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80051222-C-A

75715668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 80051222-C-T

75715806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 80051356-T-C

75715990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: 80051529-A-G

75716175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: 80051708-T-C

75716493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: 80051990-A-G

75716538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: 80052036-G-T

75717074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: 80052634-A-G

75717310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: 80052910-G-A

http://identifiers.org/hco/6/GRCh38#75717363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#80053082-C-A

75717363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: 80053082-C-G

75717459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: 80053196-T-G

75717526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: 80053262-A-G

75717548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: 80053286-G-A

75717548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: 80053286-G-T

75717594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: 80053333-C-T

75717617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: 80053356-C-T

75718104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20944
most severe consequence: 3 prime UTR variant
orthologous variants: 80053816-C-T