100031990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89663027-T-C

100032039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89662978-C-T

100032096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89662927-G-T

100032251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89662779-A-G

100032327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89662716-C-T

100032389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89662677-T-C

100032447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89662626-G-T

100032473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89662600-G-T

http://identifiers.org/hco/12/GRCh38#100032536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89662540-A-C

http://identifiers.org/hco/12/GRCh38#100032550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89662525-C-A

100032550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89662525-C-T

100032821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89662276-G-C

100032821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89662276-G-T

100034140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89658062-T-C

100034201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89658004-A-G

100034729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89657572-G-T

http://identifiers.org/hco/12/GRCh38#100034755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89657529-C-A

100034782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89657466-C-T

100035172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89655994-A-G

http://identifiers.org/hco/12/GRCh38#100035396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89655733-C-A

100035396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89655733-C-T

100035927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89655514-G-C

http://identifiers.org/hco/12/GRCh38#100036007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89655444-C-A

100036611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89654860-G-A

100036862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89654595-T-C

100036961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89654510-T-A

100037047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89654450-T-C

100037050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89654447-T-C

100037221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89654262-T-C

100037448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89654086-A-G

100037479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89654054-T-C

100037603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89653944-G-A

100037603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89653944-G-T

100037661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, missense_variant
orthologous variants: 89653889-T-C

100037730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, missense_variant
orthologous variants: 89653820-T-C

100037777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89653777-G-A

100037777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89653777-G-T

100037783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89653771-G-C

100037783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89653771-G-T

100037784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89653770-A-T

http://identifiers.org/hco/12/GRCh38#100037799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89653754-C-A

100037799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89653754-C-T

http://identifiers.org/hco/12/GRCh38#100037878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89653688-C-A

100037878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89653688-C-T

100038083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89653499-T-C

100038245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89653354-A-G

100038245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89653354-A-T

http://identifiers.org/hco/12/GRCh38#100038250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89653349-A-C

100038302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89653284-G-A

100039400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89652228-A-G

http://identifiers.org/hco/12/GRCh38#100039444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89652189-A-C

http://identifiers.org/hco/12/GRCh38#100039489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89652162-C-A

100039489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89652162-C-G

100039489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89652162-C-T

100039511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89652139-T-C

100039792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 89651897-G-C

http://identifiers.org/hco/12/GRCh38#100039806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89651883-C-A

100039806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89651883-C-G

100039806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89651883-C-T

100039821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89651865-T-A

100039821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89651865-T-C

100039836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89651849-T-C

http://identifiers.org/hco/12/GRCh38#100039848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89651838-A-C

100039856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89651830-T-A

100039891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89651797-T-C

http://identifiers.org/hco/12/GRCh38#100039924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89651765-C-A

100039924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89651765-C-T

100047544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense variant
orthologous variants: 89647998-G-A

100047547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense variant
orthologous variants: 89647995-C-T

100047574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense variant
orthologous variants: 89647968-T-C

100047613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense variant
orthologous variants: 89647929-A-G

100047642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 89647900-C-T

100047666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89647877-T-G

100047667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89647876-G-T

http://identifiers.org/hco/12/GRCh38#100048030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89647513-C-A

100048055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense variant
orthologous variants: 89647488-G-A

100048055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense variant
orthologous variants: 89647488-G-T

100048064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense variant
orthologous variants: 89647479-T-C

100048166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense variant
orthologous variants: 89647377-T-A

100048166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense variant
orthologous variants: 89647377-T-C

100048222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89647319-G-A

100048222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89647319-G-C

100048222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89647319-G-T

http://identifiers.org/hco/12/GRCh38#100048273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89647221-A-C

100048318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89647151-T-A

100048318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89647151-T-C

100048334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89647135-T-C

100048339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89647129-G-A

100048339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89647129-G-T

http://identifiers.org/hco/12/GRCh38#100048344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89647124-C-A

100048344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89647124-C-T

http://identifiers.org/hco/12/GRCh38#100048392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89647076-A-C

100048595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89646939-T-C

http://identifiers.org/hco/12/GRCh38#100048685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89646875-A-C

100048721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89646855-T-C

http://identifiers.org/hco/12/GRCh38#100048825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89646816-C-A

100048899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89646741-A-G

100050025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89645751-A-T

100050133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron variant
orthologous variants: 89645661-T-C

100050222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense variant
orthologous variants: 89645584-G-A

100050241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: synonymous variant
orthologous variants: 89645565-A-G

100050448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89645364-G-A

100050448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89645364-G-T

http://identifiers.org/hco/12/GRCh38#100050450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89645362-C-A

100050450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89645362-C-T

100050841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89644755-C-G

http://identifiers.org/hco/12/GRCh38#100050944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89644644-C-A

100050944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89644644-C-G

http://identifiers.org/hco/12/GRCh38#100050950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89644638-C-A

100050950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89644638-C-G

100050950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89644638-C-T

http://identifiers.org/hco/12/GRCh38#100050953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89644635-C-A

100051125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89644474-G-A

100051309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89644292-T-A

100051309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89644292-T-C

100051371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89644238-T-A

100051400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89644206-T-A

http://identifiers.org/hco/12/GRCh38#100057541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89642684-A-C

100057541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89642684-A-G

100057609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89642618-T-C

100057609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89642618-T-G

100057672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89642558-G-A

100057672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89642558-G-C

100057717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89642513-T-C

100057778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89642448-T-A

100057778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89642448-T-C

100057859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89642236-T-A

100057859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89642236-T-C

http://identifiers.org/hco/12/GRCh38#100057874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89642222-A-C

100057874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89642222-A-G

100057933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89642167-T-A

100057955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89642145-A-G

100057969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89642131-T-C

100058035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89642067-G-C

100058035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89642067-G-T

http://identifiers.org/hco/12/GRCh38#100058060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89642042-C-A

100058066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89642036-G-A

100058066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89642036-G-T

http://identifiers.org/hco/12/GRCh38#100058087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89642015-C-A

100058087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89642015-C-G

100058195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89641907-G-T

100058223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 89641879-A-G

100058302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89641800-A-G

100058647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89641455-T-C

100058677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89641425-G-A

100058719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89641383-G-T

100058920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89641185-T-C

100059049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89641056-G-A

100059072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 89641033-T-A

100059072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 89641033-T-C

100059076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89641029-T-C

100059181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89640924-G-A

100059191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89640914-C-G

100059191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89640914-C-T

100059241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89640864-T-G

100059406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89640699-T-C

http://identifiers.org/hco/12/GRCh38#100059539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89640566-A-C

100059539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 89640566-A-G

100059570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89640539-A-G

http://identifiers.org/hco/12/GRCh38#100059596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89640513-A-C

100060100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89638842-T-G

100060127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89638830-G-A

100060127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89638830-G-C

100060127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89638830-G-T

http://identifiers.org/hco/12/GRCh38#100060562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89638263-A-C

100061190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89636747-G-A

100061860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89636350-T-C

100069951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

100069987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

100069987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

100070012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

100070095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

http://identifiers.org/hco/12/GRCh38#100070149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

100070149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/12/GRCh38#100070229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

100070229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

100071613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89631169-T-C

100071835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89631033-C-T

100072459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89630712-C-T

100072467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89630705-G-A

http://identifiers.org/hco/12/GRCh38#100072511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89630641-A-C

100072520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89630632-A-T

100072695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89630461-T-A

100072695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89630461-T-C

100072695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89630461-T-G

http://identifiers.org/hco/12/GRCh38#100072854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89630309-A-C

100072856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89630306-A-G

100072876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89630286-C-T

http://identifiers.org/hco/12/GRCh38#100072879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89630283-C-A

100072879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89630283-C-G

100072960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89630055-C-T

100073069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89629943-T-C

100073249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89629810-T-C

100077803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89628219-T-C

http://identifiers.org/hco/12/GRCh38#100077817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89628199-C-A

100077817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89628199-C-T

100077859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89628131-G-C

100077956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89628049-C-T

100077979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89628026-A-G

100077979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89628026-A-T

100082873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89627454-G-T

http://identifiers.org/hco/12/GRCh38#100082895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89627432-A-C

100082896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89627431-T-A

100082896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89627431-T-C

100082896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89627431-T-G

100082950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89627380-A-G

100084604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89626465-C-T

http://identifiers.org/hco/12/GRCh38#100084730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89626331-C-A

100084733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89626328-T-C

100084733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89626328-T-G

http://identifiers.org/hco/12/GRCh38#100084791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89626261-C-A

100084791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89626261-C-T

100085678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89626094-T-C

100085738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89626018-T-G

100085983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89625821-C-T

http://identifiers.org/hco/12/GRCh38#100086021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89625475-A-C

100086195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89625327-A-G

100086237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89625279-A-G

http://identifiers.org/hco/12/GRCh38#100086371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89625145-A-C

100086371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89625145-A-G

100086371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89625145-A-T

http://identifiers.org/hco/12/GRCh38#100086391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89625126-A-C

100086391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89625126-A-G

100086391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89625126-A-T

100086417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89625101-T-G

100089037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89623023-G-A

100089076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89622984-G-A

100089109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89622953-A-G

100089160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89622899-T-G

100095592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89618667-T-C

http://identifiers.org/hco/12/GRCh38#100095626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89618632-C-A

100095626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89618632-C-G

100095626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89618632-C-T

100095638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89618628-G-T

100095645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89618621-T-G

http://identifiers.org/hco/12/GRCh38#100095654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89618613-C-A

100095654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89618613-C-T

100095659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 89618608-T-C

http://identifiers.org/hco/12/GRCh38#100095955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89618310-C-A

100095955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89618310-C-G

100095955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89618310-C-T

100097334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89617154-A-G

100097561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89616939-A-G

100097598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89616900-A-G

100097598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89616900-A-T

100102647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89612042-G-T

100102793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89611863-G-A

http://identifiers.org/hco/12/GRCh38#100102799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89611857-C-A

100103041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89611672-A-G

http://identifiers.org/hco/12/GRCh38#100103049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89611664-C-A

http://identifiers.org/hco/12/GRCh38#100103124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89611600-A-C

100103419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89611342-T-C

100103779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89610095-T-C

100103799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89610075-T-A

100103882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89610009-T-C

100104075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89609822-T-C

100104075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89609822-T-G

http://identifiers.org/hco/12/GRCh38#100108267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89608712-A-C

100108267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89608712-A-G

100108540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89608455-T-C

100108540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89608455-T-G

100113869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89598004-G-A

100113985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89597909-G-A

100113985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89597909-G-C

100114726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89596138-T-C

100114830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89595799-A-G

100123847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89594740-T-A

http://identifiers.org/hco/12/GRCh38#100125786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89594443-A-C

100125902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89594359-T-A

100126010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89594252-A-G

100126028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89594235-G-A

100126054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89594210-C-T

http://identifiers.org/hco/12/GRCh38#100126106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89594135-A-C

http://identifiers.org/hco/12/GRCh38#100126109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89594132-A-C

http://identifiers.org/hco/12/GRCh38#100126305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89593926-A-C

100126493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89593671-C-T

100126543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89593577-C-T

100126558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89593562-T-A

100126863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89593298-A-G

100126863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89593298-A-T

100128143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89591795-A-G

http://identifiers.org/hco/12/GRCh38#100128225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89591710-C-A

100128485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89591490-G-A

100128548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89591444-A-G

100128610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89591395-T-C

100128659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89591347-C-G

100128660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89591346-T-C

100128669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89591337-T-A

100128670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89591336-T-C

http://identifiers.org/hco/12/GRCh38#100128683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#89591323-C-A

100128683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 89591323-C-T

100128816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89591199-G-A

100128816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89591199-G-T

http://identifiers.org/hco/12/GRCh38#100128844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89591177-C-A

100128844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89591177-C-G

100128844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89591177-C-T

100128855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89591166-G-A

100128855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89591166-G-C

100128855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89591166-G-T

http://identifiers.org/hco/12/GRCh38#100129690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89590195-A-C

http://identifiers.org/hco/12/GRCh38#100137760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89585289-C-A

100138250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89584505-T-C

100138251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89584504-G-T

100138867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583870-A-T

100138872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583865-C-T

100139371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583334-T-C

100141008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582535-G-A

100141320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582247-A-G

http://identifiers.org/hco/12/GRCh38#100141377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89582228-A-C

100141389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582216-G-A

100141749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89581821-T-A

100141750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89581820-G-A

http://identifiers.org/hco/12/GRCh38#100142499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#89581183-C-A

100142499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89581183-C-T

100142720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 89581020-G-A

100142720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 89581020-G-C

100142720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 89581020-G-T

http://identifiers.org/hco/12/GRCh38#100142723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89581017-C-A

100142723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 89581017-C-T

http://identifiers.org/hco/12/GRCh38#100142802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#89580928-C-A

100142802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29102
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89580928-C-T