133038483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103638915-C-G

133038483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103638915-C-T

133038538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103638881-T-C

http://identifiers.org/hco/3/GRCh38#133038646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103638757-C-A

133038767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103638635-G-A

133038779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103638629-C-G

133039260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103638132-G-T

133039835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103637620-C-G

133039946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103637489-A-T

133040578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103637146-A-G

133040643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103637070-T-A

133040911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103636807-G-A

http://identifiers.org/hco/3/GRCh38#133041182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103636559-C-A

133041272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103636479-G-T

133041288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103636467-A-G

133041334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103636420-T-A

133041606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103635958-T-C

133041684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103635747-A-T

133041949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103635497-G-A

133041949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103635497-G-T

133042058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103635388-C-T

133042457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103634922-C-G

133042457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103634922-C-T

133042903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103634498-A-G

133042934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103634469-G-A

133043004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103634376-T-A

133043037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103634340-G-C

133043174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103634189-C-T

133043771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103632293-A-G

133043964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103632066-A-G

133045867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103630199-G-A

133045930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103630142-T-C

133045955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103630117-G-A

http://identifiers.org/hco/3/GRCh38#133045989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103630083-C-A

133045989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103630083-C-T

133046121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103629957-G-T

133046161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103629919-A-G

133046179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103629906-A-G

133046248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103629841-A-G

133046332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103629784-A-T

133046403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103629715-A-G

133046463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103629658-G-A

133046463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103629658-G-T

133046484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103629637-A-G

133046672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103629454-T-G

133046854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103629165-G-A

133046906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103629109-C-T

133046922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103629094-A-G

133046973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103629068-G-T

133047140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103628898-G-A

133047178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103628854-T-G

133047368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103628694-A-T

133047380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103628682-G-A

133047444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103628618-A-T

133047707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103628297-G-A

133047808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103628199-A-G

133047825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103628185-C-T

133047838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103628172-G-A

133049343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626845-T-C

133049404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626784-C-G

133049533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626659-G-T

133049558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626634-G-T

133049579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626623-C-G

133049745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626455-G-A

133050259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626209-G-C

133050262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626206-G-A

133050262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626206-G-T

133050285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626195-G-C

133050288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626192-T-C

http://identifiers.org/hco/3/GRCh38#133050401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103626095-A-C

133050401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626095-A-G

133050470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626036-A-G

133050585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625923-G-C

133050587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625921-A-G

133050701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625806-C-G

133051157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625380-C-T

133051452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625112-A-G

133051453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625111-T-C

133051478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625094-T-C

133051482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625089-C-G

133051514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625058-T-C

133051522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625050-C-T

133051559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625029-T-C

133051566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625022-T-G

133051579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625009-T-C

133051588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625000-T-A

133051611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103624976-T-C

133051871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103624712-A-G

133052577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103618692-C-T

133052741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103618559-G-A

133052973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103618356-G-A

133053713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103618261-T-C

133053860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103618113-C-T

133053916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103618039-G-A

133053974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103617978-C-T

133054030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103617927-G-T

133054097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103617860-G-A

133054262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103617690-A-G

http://identifiers.org/hco/3/GRCh38#133054275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103617675-A-C

133054302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103617648-G-T

133054505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103617439-C-T

133054747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103617181-T-G

133054806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103617121-C-T

http://identifiers.org/hco/3/GRCh38#133054886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103617053-A-C

133055000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103616937-G-A

133055009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103616934-A-T

133055012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103616931-T-C

133055183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103616761-A-G

133055903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103615979-C-T

133056149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103615143-C-T

133056152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103615142-C-T

133056153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103615141-T-C

133056294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103615002-T-A

133056474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103614818-C-T

133056555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103614755-G-A

133056866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103614458-T-C

133057147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103613551-G-A

133057147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103613551-G-C

133057205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103613492-A-T

133057275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103613417-T-C

http://identifiers.org/hco/3/GRCh38#133057483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103613285-A-C

133057483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103613285-A-G

133057483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103613285-A-T

133057520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103613250-T-C

133057520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103613250-T-G

133057609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103613166-C-T

133059483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103613092-T-A

133059561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103613014-G-C

133059588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103612989-C-T

133059628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103612953-C-T

133059845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103612771-G-T

133059991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103612635-C-T

133060007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103612619-C-T

133060051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103612578-A-T

133060075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103612554-C-T

http://identifiers.org/hco/3/GRCh38#133060101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103612525-C-A

133060230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103612415-G-A

133060332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103612308-G-T

133060476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103612214-A-G

133060931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103609723-G-A

133061071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103609632-A-G

133061095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103609608-A-G

133061963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103608368-T-C

133062155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103608179-C-G

133062186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103608148-C-T

133062316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103608018-T-A

133062685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103607427-T-C

133062948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103607216-G-A

133063030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103607136-G-A

133063373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103606830-A-G

133063478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103606718-G-T

133063547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103606565-A-G

http://identifiers.org/hco/3/GRCh38#133063774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103606393-C-A

133063917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103606261-G-A

133063917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103606261-G-C

133064058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103606134-T-G

133064072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103606120-A-G

133064110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103606082-T-C

133064458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605767-A-G

133064626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605599-A-G

133064683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605542-T-C

133064700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605526-G-T

133064741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605490-G-A

133064768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605463-A-G

133064858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605417-G-T

133064973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605318-G-A

133065041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605247-C-T

133065081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605210-A-G

133065108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605183-A-G

133065108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605183-A-T

133065134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605157-T-G

133065205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605093-G-C

133065241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605057-G-A

133065336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103605003-G-A

133065493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103604754-A-G

133065847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103604095-A-G

133065847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103604095-A-T

133065980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103603985-T-C

133066062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103603902-C-T

133066227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103603751-C-T

133066332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103603645-C-G

133066530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103603465-T-G

133066536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103603459-A-G

133066567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103603431-A-T

133069987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103601347-C-T

133070067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103601261-T-C

133070072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103601234-A-T

133076539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103599641-G-A

133076557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103599620-A-G

133076572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103599607-T-C

133076855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103599360-G-A

http://identifiers.org/hco/3/GRCh38#133076891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103599321-A-C

133077370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103598892-A-G

133077370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103598892-A-T

133077387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103598887-G-A

133077478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103598832-G-A

133077481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103598829-G-T

133077508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103598796-C-T

http://identifiers.org/hco/3/GRCh38#133077515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103598789-C-A

133077515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103598789-C-G

133077582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103598721-C-T

133077721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103598586-C-T

133077849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103598505-G-T

133078235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103597593-T-C

http://identifiers.org/hco/3/GRCh38#133078311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103597529-C-A

133078311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103597529-C-T

133078388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103597456-T-G

133078396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103597448-C-T

133078974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103596801-C-T

133079287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103596507-A-G

133079366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103596434-G-C

133079621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103596218-T-A

133079690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103596141-A-G

133079965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103595937-G-A

133080094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103595800-A-G

133080239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103595659-T-C

http://identifiers.org/hco/3/GRCh38#133082252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103595103-A-C

133082291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103595063-C-T

133082323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103595038-T-C

http://identifiers.org/hco/3/GRCh38#133083305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103594417-C-A

133083828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103593830-C-G

133083846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103593816-T-C

133084054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103593610-T-C

133084094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103593567-T-G

133084244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103593418-C-G

133084245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103593417-T-C

133084401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103593290-T-C

133084431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103593221-T-C

133084450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103593173-G-A

133084504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103593130-G-A

133084967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103592747-G-T

133085170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103592532-A-G

133085373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103592357-C-G

133085438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103592312-A-G

http://identifiers.org/hco/3/GRCh38#133085481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103592273-A-C

133085571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103592133-A-G

http://identifiers.org/hco/3/GRCh38#133085663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103592018-C-A

133085895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103591799-G-A

133085980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103591713-A-G

133086015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103591675-T-A

133086468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103590832-A-T

133086746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103590574-A-G

133087038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103590181-C-T

133087190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103590032-T-C

133087205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103590017-C-T

133087210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103590012-T-C

133088138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103589521-T-C

http://identifiers.org/hco/3/GRCh38#133088357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103589299-C-A

133088477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103589111-T-G

133088478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103589110-A-G

133088582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103588988-G-A

133093895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103587848-T-G

133094167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103587593-C-T

133094175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103587585-G-A

133094183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103587577-A-G

133094194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103587566-T-G

133105379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103587020-C-T

133105752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103586454-A-G

133105759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103586447-C-T

133105773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103586431-G-C

133105796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103586408-A-G

133105821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103586383-G-A

133106145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103586103-A-G

133106161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103586087-T-A

133106161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103586087-T-C

133106708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103585626-T-C

133106869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103585501-G-A

http://identifiers.org/hco/3/GRCh38#133107238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103585127-C-A

133107238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103585127-C-T

133107635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103584613-T-G

133107659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103584589-A-T

133107812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103584457-G-A

133109110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103584242-A-G

133109114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103584238-G-A

133109114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103584238-G-T

133109741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103583787-T-A

133109877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103583652-G-A

133110335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103582864-A-G

http://identifiers.org/hco/3/GRCh38#133110378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103582821-C-A

133110424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103582783-T-G

http://identifiers.org/hco/3/GRCh38#133110954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103582341-A-C

133110954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103582341-A-G

133110964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103582331-G-T

133110978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103582317-C-T

133111044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103582260-C-T

133111251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103581983-A-G

133111351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103581878-A-G

133111573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103581734-T-C

http://identifiers.org/hco/3/GRCh38#133111585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103581722-A-C

133111585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103581722-A-T

133111668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103581640-G-A

http://identifiers.org/hco/3/GRCh38#133111704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103581607-A-C

133111704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103581607-A-G

133111729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103581588-C-T

133112689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103580405-A-G

133112765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103580329-C-T

133112813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103580286-C-T

133113173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103579417-T-G

133113205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103579388-G-C

133113214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103579385-T-G

133113228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103579365-A-T

http://identifiers.org/hco/3/GRCh38#133113235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103579314-C-A

133113235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103579314-C-T

133113254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103579268-G-A

133113882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103578654-T-C

133113882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103578654-T-G

http://identifiers.org/hco/3/GRCh38#133115402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103578272-C-A

133116713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103576247-A-G

133117257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103575861-C-T

133119046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103574613-G-T

http://identifiers.org/hco/3/GRCh38#133119129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103574545-C-A

133119138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103574540-A-G

133119484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103574213-G-T

133119614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103574095-G-A

133119614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103574095-G-T

http://identifiers.org/hco/3/GRCh38#133119619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103574090-A-C

133119836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103573872-A-G

http://identifiers.org/hco/3/GRCh38#133120065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103573645-A-C

133120150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103573525-T-C

133120186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103573485-G-A

133120209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103573458-G-A

133121922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103572785-T-C

133122254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103572517-T-C

133122378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103572442-A-G

133122471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103572356-C-T

133123190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103572156-C-G

133123213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103572127-G-C

133123612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103571755-A-G

133123640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103571729-G-A

133123791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103571486-A-G

133123807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103571380-C-G

133123901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103571260-C-G

133124209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103570943-G-A

133124209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103570943-G-C

133124380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103570422-T-C

133124388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103570414-G-T

133124433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103570377-G-A

133124466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103570343-T-C

133124531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103570277-C-T

133124636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103570182-C-T

http://identifiers.org/hco/3/GRCh38#133124705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#103570111-C-A

133124725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103570091-T-C

133124759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103570057-G-A

133124759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103570057-G-T

133124885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103569929-G-A

133124885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103569929-G-C

133125005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103569763-T-C

133125099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103569648-A-G

133125122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103569625-T-A

133125122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103569625-T-G

133125329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103569410-T-G

133125503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103569232-C-T

133125686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103569047-G-A

133126012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103568408-A-G

133126058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103568362-C-T

133126080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103568340-G-A

http://identifiers.org/hco/3/GRCh38#133126149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103568272-A-C

133127418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103568017-G-A

133127540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103567904-A-G

http://identifiers.org/hco/3/GRCh38#133127661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103567807-C-A

133128068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103567428-G-A

133128098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103567387-G-T

http://identifiers.org/hco/3/GRCh38#133128273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103567197-A-C

133128273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103567197-A-G

133128746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103566811-A-T

133129155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103566495-G-A

133129705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103565746-A-T

133130408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103564985-A-T

133130428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103564966-C-T

133130718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103564682-A-G

http://identifiers.org/hco/3/GRCh38#133130720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103564680-C-A

133131114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103564288-T-C

133135117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103557279-A-T

133135137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103557259-C-T

133135149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103557247-C-T

133135157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103557239-G-T

133135220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103557170-C-G

133135220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103557170-C-T

133135287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103557108-C-T

133135302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103557093-A-G

133135433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103556851-A-G

133135603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103556681-A-G

133135723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103556545-G-T

133135861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103556416-G-A

133135929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103556366-A-G

133136136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103556190-G-A

http://identifiers.org/hco/3/GRCh38#133136267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103556057-A-C

133136367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555938-T-C

133136379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103555926-T-C

133136411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555893-A-G

133136411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555893-A-T

133136636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555688-T-C

133137069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555242-T-C

133137077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555234-T-G

133137090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555221-G-A

133137090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555221-G-T

133137116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555192-G-A

133137116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555192-G-C

133137118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555190-T-C

133137163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555148-C-T

133137176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555133-C-G

133137186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555123-T-C

133137210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103555100-A-T

133137292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103555019-G-A

http://identifiers.org/hco/3/GRCh38#133137340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103554970-A-C

133137340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103554970-A-G

133137360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103554951-T-C

133137432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103554880-C-T

133137492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103554824-G-T

133137569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103554771-A-G

133137622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103554718-A-T

133137631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103554709-G-T

133137672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103554401-C-T

133137696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103554363-T-C

133137838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103554238-T-C

133137860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103554221-C-T

133137869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103554212-T-A

http://identifiers.org/hco/3/GRCh38#133137930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103554149-A-C

133138001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103554093-T-G

133143346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103553921-C-T

133143692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103553581-A-G

133143758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103553532-G-A

133143835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103553484-C-T

133148591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103549960-T-G

133149087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103549816-G-T

133149414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103549501-A-G

133149465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103549311-C-T

133149921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103548796-G-A

133149956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103548757-T-C

133150099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103548608-C-G

133150132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103548575-A-G

133150213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103548508-T-G

133151293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103547468-A-G

133151415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103547346-G-A

http://identifiers.org/hco/3/GRCh38#133151444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103547316-C-A

133151450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103547310-T-C

133151660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103547011-C-T

133151666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103546962-T-G

133151851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103546594-A-G

http://identifiers.org/hco/3/GRCh38#133152054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103546395-A-C

133152211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103546261-T-C

133152314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103546154-A-G

133152428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103546046-G-A

133152432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103546042-C-T

133152456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103546013-T-G

133152693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103545779-C-G

133152943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103545492-A-G

133152958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103545477-A-G

http://identifiers.org/hco/3/GRCh38#133153023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103545418-C-A

133153205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103545231-C-T

133153208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103545228-A-G

133153742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103541243-G-A

133153802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103541189-G-T

133153803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103541188-G-A

133153961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103541071-G-A

133153964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103541068-G-A

133156285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103540902-G-A

133156943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103539375-G-A

133156964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103539354-T-C

133157000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103539323-G-A

133157013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103539309-A-T

133157033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103539292-C-G

133157147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103539195-G-A

133157157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103539185-T-C

133157199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103539157-A-G

http://identifiers.org/hco/3/GRCh38#133157203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103539155-A-C

133157286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103539072-G-T

133157351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103539011-A-G

133157424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103538941-T-C

133157531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103538806-G-A

133157823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103538494-T-A

133157832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103538485-G-A

133157832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103538485-G-T

133157848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103538470-G-A

http://identifiers.org/hco/3/GRCh38#133157933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103538399-A-C

133157966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103538372-T-G

133158853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103538200-T-C

http://identifiers.org/hco/3/GRCh38#133158882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103538164-C-A

133158903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103538137-G-A

133158903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103538137-G-T

133158943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103538089-G-A

133158977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103538053-C-T

133159006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103538021-A-G

http://identifiers.org/hco/3/GRCh38#133159045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103537978-C-A

133159048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103537975-C-G

133159178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103537857-G-A

133159412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103537627-G-T

133159441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103537598-T-C

133159441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103537598-T-G

http://identifiers.org/hco/3/GRCh38#133160467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103537254-C-A

http://identifiers.org/hco/3/GRCh38#133160550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103537165-C-A

133160884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103536718-A-G

133161028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103536600-C-G

133161115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103536534-A-G

133161151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103536498-G-C

133161285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103536362-T-A

133161312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103536345-C-T

133161315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103536342-G-A

133161315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103536342-G-C

133161482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103536201-A-G

133161491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103536198-A-G

133161506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103536183-A-G

133161663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103536046-G-A

133161906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103535852-G-A

133162041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103535716-G-A

133162041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103535716-G-C

133162223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103535514-A-G

133162279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103535465-C-T

133162549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103535263-G-A

133162579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103535229-T-C

133162630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103535177-T-C

133162945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103534873-A-G

133162949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103534869-A-G

133163106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103534717-C-G

133164182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103533807-T-C

133164269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103533724-T-C

133164575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103533396-A-T

http://identifiers.org/hco/3/GRCh38#133164658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103533313-A-C

http://identifiers.org/hco/3/GRCh38#133165020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103532999-C-A

133169470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103531947-G-A

133169493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103531930-G-T

133169767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103531642-G-A

133169830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103531580-G-A

133169859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103531551-C-G

133170310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103531120-A-T

133170474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103530957-G-A

133170474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103530957-G-T

133170496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103530935-G-A

133171730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103526883-G-A

http://identifiers.org/hco/3/GRCh38#133171842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103526779-A-C

133171968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103526572-T-C

133172027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103526508-A-G

133172053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103526474-T-G

133172202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103526135-A-G

133172202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103526135-A-T

133172204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103526133-G-T

133172426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103525915-C-G

133181041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103525717-G-A

133181041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103525717-G-C

133181041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103525717-G-T

133181045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103525713-T-A

133181045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103525713-T-C

133181097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103525661-T-C

133181195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103525566-G-A

133181195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103525566-G-T

133181360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103525327-G-C

133181361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103525325-G-A

133181394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103525293-T-G

133181998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103523202-G-A

http://identifiers.org/hco/3/GRCh38#133182070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103523129-C-A

133182070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103523129-C-T

133182080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103523114-A-G

133182235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103522976-G-A

133182371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103522827-T-A

133182472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103522729-G-A

133182753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103522458-C-T

133182895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103522361-C-T

133183553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103521730-G-A

133183579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103521629-G-C

133183579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103521629-G-T

133183701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103521511-C-G

133183705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103521507-T-C

133183728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103521483-C-G

133183798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103521423-G-A

133183807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103521408-T-A

133183901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103521310-G-C

133183918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103521307-G-A

133183951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103521278-G-A

133183966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103521264-A-G

133186145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103520345-A-G

133186276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103520219-A-G

133186367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103520151-A-G

http://identifiers.org/hco/3/GRCh38#133186418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103520095-C-A

133186683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103519829-A-G

133186737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103519774-C-T

133187511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103519033-A-G

133187511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103519033-A-T

133187517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103519027-A-G

133187609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103518945-G-A

http://identifiers.org/hco/3/GRCh38#133188027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103518531-C-A

133188137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103518421-G-A

http://identifiers.org/hco/3/GRCh38#133188464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103518043-A-C

http://identifiers.org/hco/3/GRCh38#133188744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103517776-C-A

133189304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103517394-A-G

133189347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103517351-G-A

133189347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103517351-G-C

133189508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103517187-T-A

http://identifiers.org/hco/3/GRCh38#133189647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103517044-A-C

133189647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103517044-A-G

133190016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103516674-G-A

133191373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103514430-C-G

133191511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103514337-C-T

133191916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103513943-T-C

133191917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103513942-G-A

133192055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103513752-T-C

133193575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103509703-A-G

http://identifiers.org/hco/3/GRCh38#133193892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103509404-A-C

133193953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103509357-T-C

133194308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103509302-T-C

133194359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103509259-T-G

133194404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103509219-A-G

133194419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103509204-A-G

133194426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103509197-C-G

133194525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103509141-A-G

133194589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103509106-C-T

133194988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103507576-A-G

http://identifiers.org/hco/3/GRCh38#133195007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103507557-C-A

133195087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103507539-A-G

133195273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103507353-C-T

http://identifiers.org/hco/3/GRCh38#133195715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103506919-C-A

133195745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103506886-T-C

133195800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103506838-G-A

133195841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103506794-A-G

133195879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103506761-C-G

133195886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103506754-C-T

133196084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103506569-A-G

133196131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103506516-A-G

133196184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103506480-G-A

133196195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103506463-T-C

133196195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103506463-T-G

133196666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103505991-G-A

133196710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103505946-T-G

133197233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103505238-G-C

133197233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103505238-G-T

133197260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103505211-G-A

133197260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103505211-G-T

133197341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103505132-C-T

133197428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103505049-G-A

133197551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103504936-C-T

http://identifiers.org/hco/3/GRCh38#133197614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103504879-C-A

133197618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103504875-T-A

133200906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103503314-T-C

133200978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103503242-A-G

133201225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103503006-C-T

133207442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103502941-C-G

133207487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103502906-T-A

133207504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103502889-C-T

http://identifiers.org/hco/3/GRCh38#133207779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103502623-C-A

133207804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103502598-T-C

133208083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103502380-A-G

http://identifiers.org/hco/3/GRCh38#133208188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103502273-C-A

133208282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103502185-A-G

133208402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103502065-G-A

133208410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103502057-G-A

133208718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103501737-T-C

133208791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103501670-C-T

http://identifiers.org/hco/3/GRCh38#133208802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103501629-C-A

133209428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103501478-T-C

http://identifiers.org/hco/3/GRCh38#133209458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103501448-C-A

133209458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103501448-C-G

133209470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103501436-G-C

133209965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103501016-T-G

133210020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103500956-A-G

133210181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103500800-A-G

133210593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103500133-T-A

133210593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103500133-T-C

133210730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103499970-G-A

http://identifiers.org/hco/3/GRCh38#133210762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103499941-A-C

133210971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103499740-C-G

133211050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103499673-G-A

133211146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103499635-T-C

133211221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103499559-C-T

133211259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103499521-C-T

133211601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103499189-A-G

133211683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103499109-C-G

133211806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103498383-A-G

133211899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103498303-G-A

133212013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103498212-A-G

133212063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103498189-T-C

133212196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103498074-C-T

133212488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103497812-T-C

133213038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103497615-A-G

133213112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103497537-A-T

133213267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103497371-G-A

133213578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103496621-T-G

133213722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103496479-A-T

133213725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103496476-C-G

133214078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103495902-G-A

133214184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103495791-A-G

133214194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103495781-C-G

133214244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103495727-A-G

133214271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103495699-T-C

133214307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103495684-T-C

http://identifiers.org/hco/3/GRCh38#133214347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103495647-C-A

133214347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103495647-C-G

133214377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103495619-C-T

133214468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103495545-G-A

133214482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103495531-C-G

133214482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103495531-C-T

133214632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103495406-T-C

133214651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103495387-T-G

133223428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103491337-C-G

133223477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103491288-T-G

133223762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103490775-A-G

133223919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103490608-T-C

133223924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103490603-G-A

133223940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103490587-G-C

133224020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103490505-T-C

133224371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103490166-T-G

133225559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103489712-C-G

133225630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103489659-A-G

133225839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103489490-G-A

133228150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103488417-A-T

133228294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103488272-A-T

133228396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103488164-T-C

133228410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103488150-T-A

133228639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103487941-C-T

133228694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103487884-G-A

133228894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103487596-G-A

133228962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103487385-G-A

133229047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103487199-C-T

133229053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103487186-G-A

133229053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103487186-G-T

133229187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103487064-G-T

http://identifiers.org/hco/3/GRCh38#133229229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103487029-C-A

http://identifiers.org/hco/3/GRCh38#133229267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103486992-C-A

133229357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103486902-T-C

133229367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103486892-A-G

133229408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103486850-G-A

133229599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103486777-T-C

133229798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103486562-T-C

133229803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103486557-C-T

133229822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103486538-T-C

133229822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103486538-T-G

133229864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103486496-G-A

133229900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103486461-C-T

133230053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103486144-G-T

133230148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103486039-T-C

http://identifiers.org/hco/3/GRCh38#133230255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103485928-C-A

133230379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103485805-A-G

133230623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103485553-C-T

133230915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103485252-C-T

133230978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103485203-T-C

133231100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103485111-A-G

133238307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103484262-G-A

133238617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103483950-C-T

133238684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103483904-C-G

133238745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103483843-T-G

133238849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103483744-C-T

133239141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103483479-T-C

133239144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103483476-C-T

133239149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103483471-C-G

133240302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103483181-T-C

133240414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103483090-G-C

133240540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103482965-T-C

133240541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103482964-C-T

133240636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103482908-A-G

133240757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103482796-C-T

133240844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103482709-A-G

133243346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103481708-G-A

133243363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103481694-A-T

133243378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103481679-T-A

133243379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103481678-G-A

133243902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103481319-G-A

133243963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103481263-G-A

http://identifiers.org/hco/3/GRCh38#133243982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103481244-A-C

133244100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103481136-G-A

133244432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103480827-C-G

133244482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103480785-T-G

http://identifiers.org/hco/3/GRCh38#133244585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103480694-A-C

133244809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103479973-C-T

133244883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103479910-G-T

http://identifiers.org/hco/3/GRCh38#133244972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103479830-A-C

133244990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103479815-G-C

133245334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103479508-C-T

133245376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103479467-G-A

133245568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103479309-G-T

133245609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103479254-G-T

133245636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103479227-G-A

http://identifiers.org/hco/3/GRCh38#133245638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103479225-C-A

133246133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103477789-T-C

http://identifiers.org/hco/3/GRCh38#133246254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103477694-C-A

133246254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103477694-C-T

133246267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103477681-A-G

http://identifiers.org/hco/3/GRCh38#133246277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103477677-C-A

http://identifiers.org/hco/3/GRCh38#133246283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103477671-C-A

133246283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103477671-C-T

http://identifiers.org/hco/3/GRCh38#133246344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103477643-C-A

133246467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103477539-T-C

133246486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103477520-A-G

133246583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103477435-T-C

http://identifiers.org/hco/3/GRCh38#133246683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103477376-C-A

133246717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103477342-G-C

133246753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103477308-T-A

133246753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103477308-T-C

133246753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103477308-T-G

133246757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103477304-G-A

133246759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103477302-G-T

133246773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103477288-A-G

133246791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103477270-T-C

http://identifiers.org/hco/3/GRCh38#133246794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103477267-C-A

133246869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103477186-A-G

133246869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103477186-A-T

133246951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103477100-C-T

http://identifiers.org/hco/3/GRCh38#133247096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103476959-A-C

http://identifiers.org/hco/3/GRCh38#133247143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103476913-C-A

133247224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103476798-C-G

133247224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103476798-C-T

133247939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103475893-G-T

http://identifiers.org/hco/3/GRCh38#133247996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103475841-C-A

133248073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103475766-C-T

133248098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103475740-C-T

133248154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103475683-A-G

133248231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103475624-A-G

http://identifiers.org/hco/3/GRCh38#133248247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103475609-A-C

133248416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103475317-G-A

133248416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103475317-G-T

133248432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103475295-T-C

133248813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474951-T-C

133248876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474887-C-T

133248982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474781-G-A

133248982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474781-G-T

133249777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103472476-T-C

133249885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103472369-A-G

133250781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103472077-A-G

133251083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471819-G-C

133251090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471812-G-A

133251135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471780-G-C

133251283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471662-G-A

133251366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471500-T-C

133251471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471298-A-G

133251509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471258-T-C

133251700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103470856-C-T

133251862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103470691-A-G

133252304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103470277-T-G

http://identifiers.org/hco/3/GRCh38#133252352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103470231-A-C

133252514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103470113-T-C

133252762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103469897-G-A

133252769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103469890-G-C

http://identifiers.org/hco/3/GRCh38#133252781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103469879-C-A

133253361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103469214-C-T

133253463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103469146-A-G

http://identifiers.org/hco/3/GRCh38#133253500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103469111-C-A

133253515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103469102-A-G

133253542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103469082-A-G

133254002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468643-T-C

133254020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468626-G-A

133254078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468592-C-T

http://identifiers.org/hco/3/GRCh38#133254232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103468553-A-C

133254261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468515-A-T

133254519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468192-T-C

133254598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468113-G-A

133254598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468113-G-C

133254635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468072-A-G

133254639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468067-T-A

133254695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103467999-T-G

133254795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103467901-T-C

133254837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103467861-G-C

133256867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466952-A-G

133256890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466931-C-T

133256957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466873-C-G

133257047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103466784-G-A

133257060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103466770-C-T

133257257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103466575-T-C

133257304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103466528-G-A

133257304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103466528-G-C

133257304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103466528-G-T

133257368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103466464-C-G

133257504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103466338-T-C

133257998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103465803-A-G

http://identifiers.org/hco/3/GRCh38#133259381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103464234-A-C

133259381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103464234-A-G

133259430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103464190-T-G

133259480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103464150-G-C

133260761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103463837-G-A

133260941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103463676-A-G

http://identifiers.org/hco/3/GRCh38#133260975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103463650-C-A

133261026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103463565-G-A

133261058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103463533-C-T

133261116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103463479-G-A

http://identifiers.org/hco/3/GRCh38#133261160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103463428-C-A

133261438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103463278-G-T

133261588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103463195-T-C

133261615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103463168-A-G

http://identifiers.org/hco/3/GRCh38#133261677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103463106-A-C

133261677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103463106-A-T

133261771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103463031-T-A

133261973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103462834-G-A

133262061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103462737-G-A

133262092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103462688-C-T

133262550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103462229-T-C

133262633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103462158-C-T

133262925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103461866-A-G

133263150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103461660-G-C

133263231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103461578-G-A

133263243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103461566-A-G

133263307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103461498-C-G

133263723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103461005-C-T

133263757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103460969-A-G

133263901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103460816-G-A

133263925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103460792-A-G

133264003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103460718-A-G

133264371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103460643-T-C

133264371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103460643-T-G

133264401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103460613-C-T

133264624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103460396-A-T

133264726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103460294-C-T

133264997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103460107-G-A

http://identifiers.org/hco/3/GRCh38#133265036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103460059-A-C

133265049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103460046-C-T

133265106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103459991-G-C

133265170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103458627-T-A

133265324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103458481-T-C

133265368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103458383-G-A

133265482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103458166-C-T

133265506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103458142-G-C

133265536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103458112-A-G

133265596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103458051-G-T

http://identifiers.org/hco/3/GRCh38#133265708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103457958-A-C

http://identifiers.org/hco/3/GRCh38#133265813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103457865-C-A

133267172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103456823-C-T

133267223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103456770-A-G

133267424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103456585-G-A

133267424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103456585-G-T

133267435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103456574-A-G

133267631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103456407-G-T

133267673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103456370-T-C

133267695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103456348-A-T

133267715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103456328-G-A

133267780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103456266-T-A

133267789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103456257-T-C

133268068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103455993-G-T

http://identifiers.org/hco/3/GRCh38#133268210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103455878-A-C

133268219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103455869-A-G

133268390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103455722-C-T

133268890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103455244-A-G

133268904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103455230-T-C

133269076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103455065-G-A

133269111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103455040-A-G

133269292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103454823-A-G

133269493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103454639-G-T

133269510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103454622-G-A

133269549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103454583-A-G

133269694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103454445-A-T

133269802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103454318-T-C

133269857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103454266-C-T

133269951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103454162-C-G

133270042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103454080-A-T

http://identifiers.org/hco/3/GRCh38#133270064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103454058-C-A

133270106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103453441-T-G

133270152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103453395-C-G

133270152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103453395-C-T

133270196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103453350-C-T

133270393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103453195-G-T

133270473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103453140-A-G

133270597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103453047-C-T

133270693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103452953-A-T

133270749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103452902-G-A

133270757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103452894-C-T

133270769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103452884-T-A

http://identifiers.org/hco/3/GRCh38#133270828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103452854-C-A

133270828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103452854-C-T

http://identifiers.org/hco/3/GRCh38#133270844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103452839-C-A

133270844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103452839-C-T

133270942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103452748-G-A

133271039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103452638-C-T

133271096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103452582-C-T

133271106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103452572-G-T

133271360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103452102-T-C

133271680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103451805-T-C

133272214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103451357-G-A

133274850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103450799-T-C

http://identifiers.org/hco/3/GRCh38#133274927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103450722-C-A

133274977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103450604-T-G

133274993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103450584-C-G

133275088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103450512-T-C

133275162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103450447-C-T

133275165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103450444-A-G

133275165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103450444-A-T

133275167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103450443-G-T

133275579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103450064-C-G

133275754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103449883-A-G

133275765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103449872-A-G

http://identifiers.org/hco/3/GRCh38#133275821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103449816-A-C

133275863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103449756-A-G

133275866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103449753-G-A

133275866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103449753-G-C

133276100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103449539-A-T

133276183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103449469-T-G

http://identifiers.org/hco/3/GRCh38#133276297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103449357-C-A

133276354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103449298-A-G

133276522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103449132-G-A

133276666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103448987-T-A

133276686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103448967-G-A

133276686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103448967-G-T

133276705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103448948-A-G

133276943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103448733-A-G

133277056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103448635-T-C

133277084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103448607-A-G

133277093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103448598-T-C

133277097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103448594-G-A

133277148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103448551-A-G

133277229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103448294-A-T

133277328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103448192-A-G

133277329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103448191-C-T

http://identifiers.org/hco/3/GRCh38#133277338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103448182-A-C

133277338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103448182-A-T

133277580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103447924-G-A

133277638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103447897-G-A

133277638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103447897-G-T

133277644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103447891-C-T

http://identifiers.org/hco/3/GRCh38#133277803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103447756-C-A

133277803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103447756-C-T

133277840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103447714-A-G

133277904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103447662-C-T

133277914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103447652-G-A

133278076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103447472-A-G

133278172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103447375-G-A

133278330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103447258-A-G

133278339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103447249-T-C

133278368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103447220-A-T

133278369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103447219-T-C

133279137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103446907-G-A

133279152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103446898-G-A

133279341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103446731-G-A

133279439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103446637-G-A

133279439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103446637-G-T

133279565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103446552-G-C

133279606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103446512-C-G

133279639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103446486-C-G

133279639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103446486-C-T

133279968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103446189-T-C

133280090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103446059-C-T

133280304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103445860-G-C

133280356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103445795-G-A

133280363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103445789-C-G

133281518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103444038-A-T

http://identifiers.org/hco/3/GRCh38#133281554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103444007-A-C

133281690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103443889-C-T

133281790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103443798-A-T

133282998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103443560-G-A

http://identifiers.org/hco/3/GRCh38#133283269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103443311-A-C

133283284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103443297-G-C

133283284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103443297-G-T

133283322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103443254-G-A

133283468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103443112-C-T

133283751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103442812-G-A

133284189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103442418-A-G

133284376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103442277-A-G

133284394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103442262-G-A

133284435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103442230-C-G

133284544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103442149-C-G

http://identifiers.org/hco/3/GRCh38#133286668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103441929-C-A

133286993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103441696-T-A

133287356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103441398-A-T

133287973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103440782-G-T

133288515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103440298-C-T

133290953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103438230-A-G

133291059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103438113-G-T

133291098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103438070-A-G

133291141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103438035-A-T

133291177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103438000-T-C

133291778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103437746-T-C

133291783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103437741-G-A

133291816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103437708-A-G

133291982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103437559-G-A

133292096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103437456-T-C

133292130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103437430-T-C

133292130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103437430-T-G

133292528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103436938-T-C

http://identifiers.org/hco/3/GRCh38#133292577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103436890-C-A

133292613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103436852-T-C

133292732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103436744-C-T

133292749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103436721-A-G

133292847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103436621-A-T

http://identifiers.org/hco/3/GRCh38#133292943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103436536-A-C

133293117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103436363-G-C

133293473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103436061-C-T

133293515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103436017-T-A

133293638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103435892-A-G

133293640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103435890-G-A

133293854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103435692-G-C

133293875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103435671-G-A

133293967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103435580-A-G

133294052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103435495-T-C

133294116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103435437-G-C

133294117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103435436-T-G

133294431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103435126-C-T

133294556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103435002-A-G

133294744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103434827-T-A

133294744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103434827-T-G

133294772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103434799-T-C

133295376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103434467-T-C

133295380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103434463-G-A

133295381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103434462-G-T

http://identifiers.org/hco/3/GRCh38#133295426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103434417-A-C

133295473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103434370-A-G

133295485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103434355-A-G

133295509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103434331-T-C

133295621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103434213-C-G

133295621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103434213-C-T

133295964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103433948-T-A

http://identifiers.org/hco/3/GRCh38#133296144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103433777-C-A

http://identifiers.org/hco/3/GRCh38#133296446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103433480-C-A

133296467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103433452-A-G

133296609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103433323-C-T

133296625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103433307-A-G

133296640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103433295-C-T

133296646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103433289-A-G

133296933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103433025-T-A

133297063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103432918-A-G

133297089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103432892-T-C

133297138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103432843-A-T

133297149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103432832-A-G

133297221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103432762-C-T

133297365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103432639-A-G

133297430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103432582-G-A

133298892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103431379-C-T

133299057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103431239-G-A

133299189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103431111-C-T

133299408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103430912-T-C

133299799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103430192-G-A

133299799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103430192-G-C

133299818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103430182-A-G

133300243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103429423-G-T

133300376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103429293-T-G

133300538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103429153-A-T

133300838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103428873-G-A

133300838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103428873-G-T

133300967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103428770-G-C

133301167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103428631-A-G

133301582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, undefined
orthologous variants: 103428183-A-G

133301650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103428116-T-C

133301787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103428003-A-G

133301872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103427935-T-C

133302174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103427728-G-A

133302195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103427707-G-A

133302269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103427626-G-T

133302352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103427578-A-G

133302850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103427244-C-G

133302850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103427244-C-T

133302898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103427200-T-C

133302960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103427156-T-A

133302960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103427156-T-G

133303255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103426740-G-A

133303255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103426740-G-T

http://identifiers.org/hco/3/GRCh38#133303288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103426679-C-A

133303486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103426479-T-C

http://identifiers.org/hco/3/GRCh38#133313601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103424991-A-C

133313869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103424745-G-C

http://identifiers.org/hco/3/GRCh38#133313913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103424701-A-C

133313992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103424622-G-A

http://identifiers.org/hco/3/GRCh38#133314018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103424596-C-A

133314686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103423955-T-C

133314727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103423914-A-G

133315016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103423681-T-G

133315141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103423560-A-G

133315429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103423280-G-A

133315459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103423250-C-G

133315492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103423207-C-G

133315685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103423017-G-C

133315896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103422853-A-G

133316082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103422700-A-G

http://identifiers.org/hco/3/GRCh38#133316367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103422493-C-A

133316492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103422379-T-A

http://identifiers.org/hco/3/GRCh38#133316860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103422042-C-A

133316860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103422042-C-T

133316979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103421922-C-T

133316997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103421898-T-C

133317048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103421847-G-C

133317104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103421809-T-C

133317114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103421799-T-C

133317293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103421666-C-T

133317466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103421513-G-T

http://identifiers.org/hco/3/GRCh38#133317711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103421291-C-A

133317711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103421291-C-T

133317788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103421199-G-A

133317788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103421199-G-T

133317876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103421144-A-G

133317884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103421136-A-G

133317907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103421128-G-T

http://identifiers.org/hco/3/GRCh38#133317908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103421127-C-A

133317966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103421073-C-G

133318348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103420645-A-T

133318427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103420564-C-T

133326262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103419685-C-T

133326331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103419619-C-G

133327743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103418046-A-G

133327779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103418006-G-A

133329330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103417672-G-A

133329431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103417573-G-A

133329766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103415910-C-G

133329852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103415807-C-G

133329914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103415733-T-A

133329946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103415699-T-C

133330438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103415207-G-A

133330535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103415118-A-G

133330548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103415105-T-C

133330840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103414669-G-A

http://identifiers.org/hco/3/GRCh38#133330988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103414534-A-C

133331605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103413297-G-T

133331606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103413296-C-G

133331655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103413250-A-G

http://identifiers.org/hco/3/GRCh38#133331678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103413228-C-A

133331679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103413227-T-A

133331679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103413227-T-G

133331693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103413209-C-T

133332559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103412513-A-G

133332892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron variant
orthologous variants: 103412212-G-C

133334519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103407401-A-G

133334577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103407353-G-A

133334615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103407314-G-A

133334744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103407189-C-G

133334797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103407136-T-A

133334797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103407136-T-C

133334828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103407102-T-G

133334856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103407077-T-C

133334880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103407054-G-A

133334959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103406987-C-T

133335024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103406914-T-C

133335471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103406459-T-C

133335571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103406358-G-A

133352975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103404244-C-G

133353217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103404083-T-G

133353394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103403883-T-C

133353436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103403840-A-G

133353608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103403335-G-A

133353637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103403309-G-A

133353693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103403252-G-A

133353693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103403252-G-T

http://identifiers.org/hco/3/GRCh38#133353856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103403111-C-A

133353872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103403095-G-A

133354000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103403002-G-A

133354052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402990-C-T

133354122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402922-G-A

133354205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402822-T-A

133354340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402718-T-C

133354361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402699-A-G

133354430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402628-T-C

http://identifiers.org/hco/3/GRCh38#133354466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103402597-A-C

133354683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402353-C-G

133354732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402295-A-G

http://identifiers.org/hco/3/GRCh38#133354849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103402172-C-A

133354849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402172-C-T

133355051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103401982-G-A

133355151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103401896-G-A

133355412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103401674-G-T

http://identifiers.org/hco/3/GRCh38#133355421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103401663-C-A

133355429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103401655-C-G

133355528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103401397-A-G

133355698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103401195-A-G

133355748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103401142-C-T

133355928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103400969-A-G

133358797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103400380-C-T

133358812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103400365-T-A

133359070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103400110-T-C

133359299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103400013-T-C

133359665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103399713-A-G

133359737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103399647-A-T

133359914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103399500-T-C

133359973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103399424-G-A

133359973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103399424-G-C

133360008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103399389-A-T

133360053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103399361-T-A

133360070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103399344-T-C

133362457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103391676-A-G

133362538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103391595-G-A

133362539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103391594-C-T

133362540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103391593-T-C

133362570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103391563-G-A

133362590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103391545-G-C

133362641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103391494-A-T

133362798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103391391-G-C

133362908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103391271-A-T

133362928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103391251-T-C

133363028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103391152-A-G

133363326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103390992-G-A

http://identifiers.org/hco/3/GRCh38#133363790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103390593-C-A

http://identifiers.org/hco/3/GRCh38#133363847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103390532-C-A

133363985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103390401-G-A

133363985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103390401-G-C

133364006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103390380-G-A

133364131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103390255-A-G

133364310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103390101-G-A

133365494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103390003-T-C

133365767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103389748-G-A

133365990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103389517-G-A

133366276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103389256-T-C

133366431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103389093-G-A

133366447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103389077-C-T

133367779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103388971-C-T

133367865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103388893-G-T

133367899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103388853-G-A

133367949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103388792-A-G

133367954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103388787-T-C

133368016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103388723-T-C

133370560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103386164-A-G

133370757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103385986-G-A

133370812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103385936-C-T

133370917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103385896-T-C

133370918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103385895-G-A

133371202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103385686-G-T

133371286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103385604-A-G

133371324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103385570-G-A

133371324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103385570-G-T

133371678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103385315-G-A

133372030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103385016-C-T

133372250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103384777-T-C

133372344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103384655-T-A

133372465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103384476-G-A

133372465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103384476-G-T

http://identifiers.org/hco/3/GRCh38#133372652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103384281-A-C

133372882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103384073-T-A

133372882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103384073-T-C

133373053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103383912-A-T

133375297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382267-T-C

133375347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382226-C-T

133376141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103380318-A-G

133376339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103380134-T-C

http://identifiers.org/hco/3/GRCh38#133376518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103379936-C-A

133377468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379491-G-A

133377468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379491-G-T

133377507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379452-A-T

133378098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379291-A-G

133378221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379200-T-A

133378221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379200-T-C

133378227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379194-T-C

http://identifiers.org/hco/3/GRCh38#133378242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103379180-C-A

133378242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379180-C-T

http://identifiers.org/hco/3/GRCh38#133378246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103379176-C-A

133378246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379176-C-T

http://identifiers.org/hco/3/GRCh38#133378264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103379159-C-A

133378264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379159-C-T

http://identifiers.org/hco/3/GRCh38#133378266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103379157-C-A

133378287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379136-G-T

133378334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103379101-C-T

http://identifiers.org/hco/3/GRCh38#133378345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103379090-C-A

133378345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103379090-C-T

133378366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103379069-C-G

133378428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103378903-A-G

133378448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103378887-T-G

133378464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103378879-T-C

133378470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103378873-T-C

133378492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103378853-A-G

http://identifiers.org/hco/3/GRCh38#133378554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103378798-C-A

133378554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103378798-C-G

http://identifiers.org/hco/3/GRCh38#133378566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103378786-A-C

133378566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378786-A-G

133378599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378753-G-A

133378600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378752-T-C

http://identifiers.org/hco/3/GRCh38#133378782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103378408-C-A

133378833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378358-A-T

133378835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378356-G-A

133378835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378356-G-T

133378838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378353-T-C

133378921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378271-T-C

133378955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378234-G-A

133379073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378119-T-C

133379082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103378110-G-A

133379448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377701-C-T

133379575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377580-A-G

http://identifiers.org/hco/3/GRCh38#133379582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103377573-C-A

133379623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377535-A-G

133379623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377535-A-T

133379637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377521-A-G

133379637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377521-A-T

133379649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377509-G-A

133379649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377509-G-T

133379688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103377467-G-A

133379738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377419-G-A

133379862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377295-G-A

http://identifiers.org/hco/3/GRCh38#133379929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103377228-C-A

133379929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377228-C-G

133379929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377228-C-T

133380029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103377128-C-T

133380037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377120-C-G

133380046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377111-C-G

133380046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377111-C-T

133380121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103377036-C-T

133380126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103377031-C-T

133380202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376955-G-T

http://identifiers.org/hco/3/GRCh38#133380336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103376821-C-A

133380393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376764-G-A

133380393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376764-G-C

133380424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376733-G-A

133380436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 103376721-G-A

133380481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376676-C-G

133380582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376575-T-A

133380694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376466-G-C

http://identifiers.org/hco/3/GRCh38#133380871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103376289-C-A

133380871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376289-C-T

133380963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376197-C-G

133380963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103376197-C-T

http://identifiers.org/hco/3/GRCh38#133381074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103376086-A-C

133381219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103375947-C-T

133381237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103375929-G-T

http://identifiers.org/hco/3/GRCh38#133381311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103375875-C-A

133381311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103375875-C-G

133381584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103375666-C-G

133381604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103375646-C-T

133381637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103375614-C-T

http://identifiers.org/hco/3/GRCh38#133381653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103375598-A-C

133382080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103375179-G-T

133383717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372575-G-A

133383723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372569-T-G

133383742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372551-G-A

133383783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372510-G-T

133384038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372307-C-T

133384154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372196-C-T

133384296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103372091-G-T

133384600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103371787-G-T

133384602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103371785-G-C

133384755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103371646-C-T

133384778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103371623-C-T

133384866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103371548-A-T

133384923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103371487-G-A

133385818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103370329-T-C

133385833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103370310-C-T

133385956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103370191-G-T

133386048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103370114-A-G

133386085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103370089-G-A

133386111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103370058-T-C

133386121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103370047-G-A

133386247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369882-A-G

133386247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369882-A-T

133386255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369874-G-C

133386348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369805-A-G

133386382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369770-C-T

133386406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369746-C-G

133386406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369746-C-T

133386432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369720-A-G

133386516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369660-T-C

133386567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369617-C-T

http://identifiers.org/hco/3/GRCh38#133386568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103369616-A-C

133386568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369616-A-G

http://identifiers.org/hco/3/GRCh38#133386602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103369579-C-A

133386621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369560-T-A

133386633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369544-G-C

http://identifiers.org/hco/3/GRCh38#133386668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103369509-C-A

133386668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369509-C-G

133386668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369509-C-T

133386681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369498-T-C

133386789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369401-A-G

133386790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369400-A-G

http://identifiers.org/hco/3/GRCh38#133386811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103369379-C-A

133386811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369379-C-T

133386844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369346-A-G

133386907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369294-G-T

133386979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369226-G-A

133386983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369223-G-T

133387037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369191-G-T

http://identifiers.org/hco/3/GRCh38#133387076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103369155-C-A

133387076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369155-C-T

133387500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369026-T-C

133387501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103369025-G-A

http://identifiers.org/hco/3/GRCh38#133387550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103368991-C-A

133387550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368991-C-T

133387551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368988-G-A

133387551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368988-G-T

http://identifiers.org/hco/3/GRCh38#133387581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103368964-C-A

133387592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368953-A-G

http://identifiers.org/hco/3/GRCh38#133387600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103368945-C-A

133387600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368945-C-G

133387600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368945-C-T

http://identifiers.org/hco/3/GRCh38#133387614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103368932-C-A

133387614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368932-C-G

http://identifiers.org/hco/3/GRCh38#133387632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103368915-C-A

133387632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368915-C-T

133387669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368878-G-C

http://identifiers.org/hco/3/GRCh38#133387692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103368876-C-A

133387692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368876-C-G

133387734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368840-T-A

133387757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368819-C-T

133387893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368685-T-C

133387921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368658-G-A

133387921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368658-G-C

http://identifiers.org/hco/3/GRCh38#133387983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103368611-C-A

133387983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368611-C-T

133388041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368554-G-T

http://identifiers.org/hco/3/GRCh38#133388047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103368548-C-A

133388047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368548-C-T

133388144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368478-A-G

133388161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368459-T-C

http://identifiers.org/hco/3/GRCh38#133388165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103368455-A-C

133388198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368420-A-G

133388221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368397-C-G

133388221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368397-C-T

133388294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368328-G-C

133388294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368328-G-T

133388393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368285-G-A

133388425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368253-C-T

133388503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368203-A-G

http://identifiers.org/hco/3/GRCh38#133388583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103368142-C-A

133388614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368109-A-G

133388616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368107-A-G

http://identifiers.org/hco/3/GRCh38#133388684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103368035-C-A

133388718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368005-G-C

133388718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368005-G-T

133388720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103368003-G-T

133388730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103367993-G-T

133388800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103367943-G-A

http://identifiers.org/hco/3/GRCh38#133388838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103367916-C-A

133388838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103367916-C-T

http://identifiers.org/hco/3/GRCh38#133388867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103367892-C-A

133388867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103367892-C-G

133388867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103367892-C-T

133388879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103367880-T-C

133388965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103367797-G-A

133388965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103367797-G-C

133388965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103367797-G-T

133390353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103366378-C-T

133390368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103366360-G-A

133390383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103366345-A-G

133390433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103366300-A-G

http://identifiers.org/hco/3/GRCh38#133390438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103366295-C-A

133390440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103366292-A-G

133390546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103366183-T-G

http://identifiers.org/hco/3/GRCh38#133390693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103366037-C-A

133393075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364483-C-T

133393277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103364318-C-T

133393778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103363921-T-C

133394042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103363659-T-C

133394153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103363534-C-T

133394195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103363496-T-C

133394463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103363314-T-G

133394602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103363178-C-G

http://identifiers.org/hco/3/GRCh38#133394704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103363094-A-C

133394780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103363018-C-G

133394894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103362876-A-T

133395068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103362701-G-A

133395070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103362699-A-G

133395196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103362575-T-C

133395208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103362556-C-T

133395217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103362547-C-T

133395508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103362272-C-T

133395818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103362025-T-C

133395818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103362025-T-G

133395828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103362015-T-A

133395828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103362015-T-C

133395897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103361947-G-T

133396316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361535-G-A

133396316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361535-G-T

http://identifiers.org/hco/3/GRCh38#133396317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103361534-A-C

133396317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361534-A-T

133396385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361466-G-T

133396441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361410-G-A

133396441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361410-G-T

133396515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361355-G-T

133396603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361310-G-T

133396681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361223-G-A

133396681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361223-G-T

133396690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361214-C-T

133396726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361178-C-T

133396784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361123-G-A

133396784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361123-G-T

133396884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103361045-G-T

133396948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103360983-G-A

133397072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103360871-T-C

http://identifiers.org/hco/3/GRCh38#133397105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103360818-C-A

133397105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103360818-C-T

133397106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28451
most severe consequence: 3 prime UTR variant
orthologous variants: 103360817-T-C