145110901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80427388-A-G

145110935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80427344-A-G

145111123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80427158-A-G

145111123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80427158-A-T

145111910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80426376-A-T

http://identifiers.org/hco/4/GRCh38#145112104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#80426178-C-A

http://identifiers.org/hco/4/GRCh38#145112142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#80426141-C-A

http://identifiers.org/hco/4/GRCh38#145112157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#80426129-C-A

145112157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80426129-C-G

145112170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80426116-A-T

http://identifiers.org/hco/4/GRCh38#145112181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#80426107-A-C

145112181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80426107-A-G

145112342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80425960-T-A

145112342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80425960-T-C

145112574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80425741-A-G

145115996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80420811-G-T

http://identifiers.org/hco/4/GRCh38#145116007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#80420803-C-A

145116007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80420803-C-G

145117172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80420315-T-C

145117220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80420284-T-C

145118785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80418289-T-C

145118881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80418196-C-G

145118881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80418196-C-T

145120710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80416357-A-G

145120928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80416171-A-G

145120928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80416171-A-T

145121128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80416030-A-G

145121157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80416011-A-G

145121157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80416011-A-T

145121442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80415706-C-T

145121471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80415677-A-G

145121471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80415677-A-T

145121475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80415673-T-G

145121560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80415603-A-G

145122131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80415249-C-T

145122215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80415210-A-G

145122697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80414826-G-C

145122697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80414826-G-T

145123030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80414623-C-T

145123039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 80414614-C-T

http://identifiers.org/hco/4/GRCh38#145123135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#80414518-C-A

145123197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80414451-C-G

145123248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80414400-G-A

145123391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80414255-T-A

145123391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80414255-T-C

145123550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 80414118-T-C

145123581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80414087-A-G

145123743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80413869-G-A

145123743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80413869-G-T

145123768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80413849-T-A

145123841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80413801-G-A

145123841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80413801-G-T

http://identifiers.org/hco/4/GRCh38#145123845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#80413797-C-A

145123845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80413797-C-G

145123845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80413797-C-T

145124024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80413704-T-A

145124024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80413704-T-C

145125033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80412640-C-G

145125055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80412618-A-T

145127577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80411853-G-A

145127577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80411853-G-T

145127594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80411840-T-C

145127702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80411745-A-G

145127718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80411728-G-A

145127718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80411728-G-T

145127848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80411612-T-C

145127890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80411572-A-G

http://identifiers.org/hco/4/GRCh38#145127891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80411571-A-C

145127914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80411549-T-C

145127931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80411532-G-T

http://identifiers.org/hco/4/GRCh38#145127970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80411496-A-C

145127972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80411494-T-A

145128137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80411352-T-C

145128191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80411294-A-G

145128204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80411281-G-T

145128332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80411195-G-A

145128362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80411165-G-T

http://identifiers.org/hco/4/GRCh38#145128376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80411151-C-A

145128729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80410486-A-G

145128733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80410482-A-G

145129499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80409789-A-T

145129528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80409778-C-T

145129550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80409760-C-T

http://identifiers.org/hco/4/GRCh38#145134087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80403861-A-C

http://identifiers.org/hco/4/GRCh38#145134139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80403784-C-A

145134139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80403784-C-T

145134390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80403553-A-G

145134563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80403383-T-C

145134615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80403332-G-A

http://identifiers.org/hco/4/GRCh38#145134631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80403316-C-A

145134755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80403211-A-G

http://identifiers.org/hco/4/GRCh38#145134780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80403186-C-A

145134888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80403084-G-A

145134888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80403084-G-T

http://identifiers.org/hco/4/GRCh38#145135027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80402952-A-C

145135027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80402952-A-T

145135318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80402690-T-A

145135477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80402543-T-C

145135567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80402450-G-A

145135594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80402428-G-T

145135630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80402393-A-G

145135686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80402338-C-T

145135893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80402129-A-T

145135937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80402085-A-T

145135956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80402066-T-C

145136242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80401773-G-C

145136350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80401674-A-G

http://identifiers.org/hco/4/GRCh38#145137074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80400935-A-C

145137074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80400935-A-G

145137314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80400718-G-A

http://identifiers.org/hco/4/GRCh38#145137421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80400618-C-A

145137421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80400618-C-T

http://identifiers.org/hco/4/GRCh38#145137561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80400478-A-C

145137561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80400478-A-G

145137561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80400478-A-T

http://identifiers.org/hco/4/GRCh38#145137575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80400464-A-C

145137624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80400415-T-G

145137859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80400183-T-C

145137953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80400089-G-C

145137953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80400089-G-T

145137995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80400050-C-T

145138357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80399688-T-C

145138526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 80399519-T-C

145138796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80399275-G-A

145138796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80399275-G-T

145139723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80398059-A-G

http://identifiers.org/hco/4/GRCh38#145139904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80397762-C-A

145139974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80397690-A-G

145139998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80397666-A-G

145139998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80397666-A-T

145140013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80397651-T-A

145140013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80397651-T-C

http://identifiers.org/hco/4/GRCh38#145140087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80397581-C-A

145140087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80397581-C-G

http://identifiers.org/hco/4/GRCh38#145141303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80396885-A-C

145141303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80396885-A-T

http://identifiers.org/hco/4/GRCh38#145141352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80396833-C-A

145141352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80396833-C-T

145141578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80396606-T-C

145141578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80396606-T-G

145141749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80396441-T-C

http://identifiers.org/hco/4/GRCh38#145141787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80396415-C-A

http://identifiers.org/hco/4/GRCh38#145141876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80396341-C-A

145141876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80396341-C-G

145142017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80396194-A-G

http://identifiers.org/hco/4/GRCh38#145142089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80396148-C-A

145142089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80396148-C-G

145142124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80396115-C-T

145142318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80395917-A-G

145142342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80395893-A-G

145142342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80395893-A-T

145142808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80395584-A-G

145142986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80395461-T-C

145142991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80395456-A-G

http://identifiers.org/hco/4/GRCh38#145143270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80395210-C-A

145143270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80395210-C-T

145143347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80395153-A-G

145143407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80395099-T-C

http://identifiers.org/hco/4/GRCh38#145143436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80395070-C-A

145143467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80395045-A-G

http://identifiers.org/hco/4/GRCh38#145143554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80394992-C-A

145143554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80394992-C-T

145143976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80394253-C-T

145143977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80394252-A-G

145144017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80394210-A-G

145144017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80394210-A-T

145144094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80394172-T-C

145144229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80394096-G-C

145144229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80394096-G-T

145144234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80394091-T-C

145144243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80394082-T-A

http://identifiers.org/hco/4/GRCh38#145144391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80393386-C-A

http://identifiers.org/hco/4/GRCh38#145144494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80393294-A-C

145144494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80393294-A-T

145144502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80393286-T-C

http://identifiers.org/hco/4/GRCh38#145144542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80393247-C-A

145144744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80393048-A-T

145144954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80392864-G-A

145145155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80392730-C-G

145145283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80392603-C-T

145145355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80392570-A-G

145145913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80392181-G-A

145145951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80392143-A-G

145145979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80392117-T-A

145145979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80392117-T-C

145146016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80392084-G-A

145146016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80392084-G-T

145146113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80391910-A-G

http://identifiers.org/hco/4/GRCh38#145146124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80391899-A-C

145146124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80391899-A-G

145146146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80391882-T-G

145146391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80391646-G-A

145146391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80391646-G-C

http://identifiers.org/hco/4/GRCh38#145146521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80391572-C-A

145146560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80391530-C-T

145146577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80391513-T-C

145150319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80390892-T-C

145150461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80390771-A-G

145150496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80390755-A-T

145150575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80390676-T-C

http://identifiers.org/hco/4/GRCh38#145150615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80390636-C-A

145150621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80390627-G-A

145150621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80390627-G-T

145150639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80390609-G-A

145150639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80390609-G-C

145150648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80390600-G-A

145150673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80390575-G-C

http://identifiers.org/hco/4/GRCh38#145150742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80390508-A-C

145150912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80390345-A-G

http://identifiers.org/hco/4/GRCh38#145151019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80389570-A-C

145151019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80389570-A-G

145151153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80389452-T-C

145151273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80389339-T-C

145151490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80389185-C-T

http://identifiers.org/hco/4/GRCh38#145151495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80389180-C-A

145151495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80389180-C-T

145151974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80388554-G-A

145152008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80388524-A-G

145152111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80388422-C-T

145152112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80388421-G-A

145152444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80387856-T-C

145155620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80385877-G-A

145155620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80385877-G-C

http://identifiers.org/hco/4/GRCh38#145155682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80385815-A-C

http://identifiers.org/hco/4/GRCh38#145155695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80385798-A-C

145155695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80385798-A-G

145155794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80385709-T-A

145155837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80385665-G-A

145155837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80385665-G-T

145157726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80384094-T-A

145157819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80384019-T-C

145158252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80383658-G-A

145158281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80383633-G-C

http://identifiers.org/hco/4/GRCh38#145158486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80383299-A-C

145158540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80383215-A-G

145159135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80382721-A-G

145159153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80382703-G-A

145159153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80382703-G-T

http://identifiers.org/hco/4/GRCh38#145159177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80382684-A-C

145159350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80382534-A-G

145159773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80382166-A-G

145159803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80382136-G-A

145159925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80382033-C-G

145160035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80381930-A-T

145160115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80381866-G-A

145160180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80381800-T-C

145160212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80381767-T-C

145160216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80381763-C-T

145160244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80381734-A-G

145161612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80380369-C-G

145161821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80380190-C-T

145161866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80380142-T-A

145162595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80380123-A-G

145162666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80380045-T-C

145162833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80379892-G-C

145162833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80379892-G-T

145162852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80379875-T-A

http://identifiers.org/hco/4/GRCh38#145162962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80379658-A-C

145163176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80378938-T-C

http://identifiers.org/hco/4/GRCh38#145163212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80378902-A-C

145163212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80378902-A-G

145163360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80378750-A-T

http://identifiers.org/hco/4/GRCh38#145163375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80378739-C-A

145163436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80378674-G-A

145164066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80378469-T-A

145164066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80378469-T-G

145164087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80378442-G-A

145164333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80378211-A-G

145165067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80377769-T-C

145166230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80376929-A-T

http://identifiers.org/hco/4/GRCh38#145168377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80375261-C-A

http://identifiers.org/hco/4/GRCh38#145168379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80375259-C-A

145169005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80374836-G-C

145169015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80374826-T-C

145171566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80373063-G-A

145171566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80373063-G-C

145171566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80373063-G-T

145171578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80373051-T-C

145171609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80373025-A-T

145171674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80372971-G-A

145171674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80372971-G-T

http://identifiers.org/hco/4/GRCh38#145171852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80372630-A-C

http://identifiers.org/hco/4/GRCh38#145171960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80372529-A-C

145172070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80372429-G-A

145172542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80372050-C-G

145172561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80372031-A-T

145176762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80369440-T-C

145177162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80369053-A-G

145178464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80367884-G-T

http://identifiers.org/hco/4/GRCh38#145178495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80367842-A-C

145178495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80367842-A-G

145178606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80367726-A-T

145178833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80367590-G-A

145179217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80367162-C-T

145179480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80366909-G-T

http://identifiers.org/hco/4/GRCh38#145179751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80366735-C-A

145179751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80366735-C-G

145179840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80366666-C-T

http://identifiers.org/hco/4/GRCh38#145179914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80366592-C-A

145179914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80366592-C-G

145179914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80366592-C-T

145179929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: synonymous_variant, undefined
orthologous variants: 80366577-G-A

145179929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: synonymous_variant, undefined
orthologous variants: 80366577-G-T

145179948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense_variant, undefined
orthologous variants: 80366558-T-C

145179960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense variant
orthologous variants: 80366546-A-G

145179960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: missense variant
orthologous variants: 80366546-A-T

145180000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 5 prime UTR variant
orthologous variants: 80366509-G-A

145180000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 5 prime UTR variant
orthologous variants: 80366509-G-C

145180077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 5 prime UTR variant
orthologous variants: 80366432-G-A

http://identifiers.org/hco/4/GRCh38#145180090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#80366413-C-A

145180090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 5 prime UTR variant
orthologous variants: 80366413-C-G

145180090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 5 prime UTR variant
orthologous variants: 80366413-C-T

145180162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 5 prime UTR variant
orthologous variants: 80366329-T-A

145180182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 80366309-G-A

145180182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 80366309-G-T

145180371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24949
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 80366203-G-C