98142618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121272526-G-A

98142618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121272526-G-T

http://identifiers.org/hco/13/GRCh38#98142637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121272549-C-A

98142637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121272549-C-T

98142669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121272579-G-T

http://identifiers.org/hco/13/GRCh38#98142765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#121272647-C-A

98142765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121272647-C-T

98142770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121272652-T-C

98142855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121272725-G-A

98142857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121272727-G-A

98142857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121272727-G-T

98142871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121272741-G-A

98142871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121272741-G-T

http://identifiers.org/hco/13/GRCh38#98142905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121272775-C-A

98142915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272788-G-C

98142915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272788-G-T

http://identifiers.org/hco/13/GRCh38#98143032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121272908-C-A

98143032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121272908-C-T

http://identifiers.org/hco/13/GRCh38#98143157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121273040-C-A

98143157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121273040-C-G

98143157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121273040-C-T

98143232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121273116-C-G

98143232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121273116-C-T

http://identifiers.org/hco/13/GRCh38#98143246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#121273130-C-A

98143246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121273130-C-T

http://identifiers.org/hco/13/GRCh38#98143276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121273160-A-C

98143333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121273217-A-G

98143339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121273223-C-T

98143388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121273264-T-C

http://identifiers.org/hco/13/GRCh38#98143390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121273266-A-C

98143540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121273385-G-A

98143540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121273385-G-T

98143608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121273445-G-A

98143608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121273445-G-C

98143608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121273445-G-T

http://identifiers.org/hco/13/GRCh38#98143639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121273480-C-A

98143903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121273719-G-C

98143926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121273742-G-T

98144049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121273853-C-G

98144062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121273865-A-G

98144113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121273924-G-T

98144177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121273987-G-A

98144281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274051-G-C

98144377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274141-T-G

98144437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274205-C-G

98144437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274205-C-T

98144621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274399-G-T

98144662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121274441-C-G

98144662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121274441-C-T

98145011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121274778-T-G

98145249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121275003-C-G

98146734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121275865-A-G

98146744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121275877-G-A

98146744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121275877-G-C

http://identifiers.org/hco/13/GRCh38#98146782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121275969-C-A

98146782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121275969-C-T

98146901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276198-T-A

98147231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276522-C-T

98147310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276590-T-G

98147333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121276615-G-A

98147509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276787-G-A

98147670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121276957-T-C

98148034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121277157-A-G

98150732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121280102-C-T

98152396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121281166-T-C

98152637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121281387-A-G

98155957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121288905-G-A

98155977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121288925-C-T

98156073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121289029-C-T

98160734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121290013-G-C

98160811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121290075-C-T

98161600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121290544-G-T

98162285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121290854-A-G

98162287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121290856-G-C

98162569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291040-A-G

98162600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291071-C-G

98162608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291080-T-C

98162609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291081-G-A

98162610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291082-G-T

98162621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291093-T-A

98162648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291148-C-T

98162652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291152-T-C

98163702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291374-C-T

98164213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121291613-G-C

98170818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298032-T-C

98170987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298229-T-G

98171062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298290-G-T

98171255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298477-A-G

http://identifiers.org/hco/13/GRCh38#98171272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121298502-A-C

http://identifiers.org/hco/13/GRCh38#98171273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121298503-C-A

http://identifiers.org/hco/13/GRCh38#98171550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121298746-C-A

98171601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298802-G-A

98171629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298830-C-G

98171629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121298830-C-T

98172249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299366-G-A

98172327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299433-G-T

http://identifiers.org/hco/13/GRCh38#98172500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121299595-A-C

98172500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299595-A-G

98172537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299624-T-C

98172577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299666-G-A

98172591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299680-C-T

98172803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299883-A-T

98172804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121299884-G-C

98173050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121300134-G-T

98173182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121300355-C-T

98174376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121302121-T-G

98174434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121302183-C-G

98174527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121302274-A-G

98174649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121302395-T-C

98181545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121307193-T-C

98181785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121307367-T-C

98181857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121307450-C-T

98181860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121307453-A-G

98182040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121307614-T-C

98182040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121307614-T-G

98183293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121308634-C-T

98183337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121308673-T-C

98183674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121308919-G-A

98183676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121308921-T-C

98183686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121308931-A-T

http://identifiers.org/hco/13/GRCh38#98183780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121309122-C-A

98183879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121309220-G-C

98183914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121309253-G-C

98183933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121309272-G-A

98183937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121309276-G-A

98183977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121309314-A-G

98184077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121309836-G-A

98187154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121312431-T-C

http://identifiers.org/hco/13/GRCh38#98187155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121312432-C-A

98187305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121312590-A-G

98187532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121312823-T-C

98187673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121312952-A-G

98187710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121312979-G-A

98187723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121312982-G-A

98188043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121313298-C-G

98188043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121313298-C-T

98188226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121313476-T-G

98188648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121313554-G-C

98188740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121313645-C-G

98188740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121313645-C-T

98188968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121313830-C-T

98189027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121313863-A-G

98189200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121314024-A-G

98189464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121315342-A-G

98189486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121315367-A-T

98189609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121315485-A-G

98190152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121315914-G-C

98190152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121315914-G-T

http://identifiers.org/hco/13/GRCh38#98190264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121316035-C-A

98191170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121317580-G-A

98191219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121317608-C-T

98191233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121317622-G-A

98191304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121317692-G-A

http://identifiers.org/hco/13/GRCh38#98193861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121320301-C-A

98196720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121325196-A-G

98198041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121326054-T-A

98198349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121326383-T-G

http://identifiers.org/hco/13/GRCh38#98202193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121330152-C-A

98202193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121330152-C-T

98202270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121330234-A-G

98202379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121330342-G-A

98202390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121330355-G-A

98202434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121330399-C-T

98202622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121330591-A-G

98202628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121330597-G-A

98206694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121335281-C-T

http://identifiers.org/hco/13/GRCh38#98207258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#121335796-C-A

http://identifiers.org/hco/13/GRCh38#98207427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121335972-A-C

98207475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121336014-G-A

98207789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121336233-A-G

http://identifiers.org/hco/13/GRCh38#98207977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121336345-C-A

98207979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121336347-T-C

98207979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121336347-T-G

98212534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121338715-G-A

98212577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121338760-A-G

98212699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121338878-C-T

98212718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121338905-G-C

98213169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121339337-G-A

98213169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121339337-G-C

98213174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121339350-T-C

98213177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121339358-T-C

http://identifiers.org/hco/13/GRCh38#98213203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121339384-C-A

98213203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121339384-C-G

98213203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121339384-C-T

98213365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: synonymous variant
orthologous variants: 121339546-C-T

http://identifiers.org/hco/13/GRCh38#98213460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121339623-C-A

98213513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121339678-T-C

98213655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121339834-C-T

98213675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121339854-A-T

98213710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121339916-T-C

98213848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121340100-C-T

98214065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121340287-G-A

98214431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121340595-C-T

98214639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121340794-A-G

98214984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121341119-T-G

98215058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121341190-T-C

98215083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121341212-C-T

http://identifiers.org/hco/13/GRCh38#98216105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121342322-A-C

98216105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121342322-A-G

98216327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121342556-G-T

98216910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121343285-G-A

98217017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121343402-C-G

98217171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121343517-A-G

98217212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121343558-A-G

98217299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121343609-T-C

98217314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121343623-A-G

98217452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121343693-C-T

98217638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121343860-A-G

98217676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121343896-A-G

98217688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121343908-G-A

98217688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121343908-G-T

98217695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121343915-T-G

98217718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121343939-G-A

98217741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121343962-T-C

98217813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121344074-G-T

http://identifiers.org/hco/13/GRCh38#98217872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121344137-C-A

98218462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121344763-T-C

98218627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121345083-A-T

98218650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121345109-G-A

98219992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121345729-T-A

98220077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121345801-G-A

98220301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121345866-G-A

98220757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121346295-G-A

98220913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121346453-T-A

98221268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121346749-C-T

98221635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121347810-G-A

http://identifiers.org/hco/13/GRCh38#98221649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121347823-C-A

98221649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121347823-C-T

98221650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121347824-G-A

98222045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121348169-T-A

98222244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121348364-G-A

98222244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121348364-G-C

98222438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121348574-G-A

98222495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121348629-C-G

98223084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121348807-C-G

98223154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121348892-C-T

98223236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121348966-C-G

98223236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121348966-C-T

http://identifiers.org/hco/13/GRCh38#98223715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121349428-A-C

98223804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121349510-C-T

98223816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121349522-T-G

98223886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121349584-G-T

98225577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121351177-C-T

98225799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121351392-C-G

98226041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121351590-G-A

http://identifiers.org/hco/13/GRCh38#98227260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121352986-C-A

98227260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121352986-C-T

98227261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121352987-G-A

98227313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121353038-G-C

98227313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121353038-G-T

98227330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121353056-A-G

98227684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121353393-T-C

98227742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121353445-G-A

98227754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121353516-G-A

98228055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121353845-G-A

http://identifiers.org/hco/13/GRCh38#98228602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121354100-C-A

98228602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121354100-C-T

98228707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121354206-T-A

98228836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121354325-A-G

98229023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121354651-G-T

98229163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121354760-C-T

98229175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121354772-A-G

98229263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121354851-A-G

98232333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121356246-T-C

98232839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121356369-A-T

98232875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121356414-A-G

98232922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121356461-C-G

98232930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121356469-G-C

98232937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121356476-T-C

98232937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121356476-T-G

98232964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121356503-A-G

98233053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121356590-A-G

98233066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121356603-G-C

98233114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121356652-C-T

http://identifiers.org/hco/13/GRCh38#98233286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121356804-C-A

98233286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121356804-C-T

98233319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121356837-A-G

98233675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357262-T-A

http://identifiers.org/hco/13/GRCh38#98233716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121357305-C-A

98233776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357367-A-G

98233805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357394-C-T

98233849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357425-G-A

98233849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357425-G-C

98233849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357425-G-T

98233931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357504-A-G

98233983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357559-G-A

98233983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357559-G-T

98233998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357572-G-A

98233998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357572-G-T

98234022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357597-G-A

98234128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357680-G-A

98234128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357680-G-T

98234135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357687-A-G

98234226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121357732-T-C

98244067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121365662-C-T

98244173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121365787-A-G

98244180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121365794-A-G

98244762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121366948-A-G

http://identifiers.org/hco/13/GRCh38#98244928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121367070-C-A

98244928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121367070-C-G

98244929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121367071-T-C

98244929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121367071-T-G

98245053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121367195-T-C

98245141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121367288-G-T

98245216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121367358-A-G

98245297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121367443-T-G

98245395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121367536-T-C

98245400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121367541-T-C

98245400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121367541-T-G

98245475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121367600-A-G

98245513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121367633-C-T

98246640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121368613-A-G

98246743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121368690-A-T

98247488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121369309-C-T

98247576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121369398-G-C

98247648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121369454-A-G

98247666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121369471-G-A

98247666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121369471-G-T

98247697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121369499-C-T

98247730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121369536-G-A

98247920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121369668-T-C

98248305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121370041-G-A

98248324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121370060-G-T

98248444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121370115-A-G

98248474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121370139-A-G

98248479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121370144-T-G

98248517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121370182-A-G

98248615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121370290-G-A

98248681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121370342-A-T

98248777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121370432-T-A

98248811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121370468-C-T

98248975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121370617-C-T

http://identifiers.org/hco/13/GRCh38#98249023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121370666-C-A

98249023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121370666-C-T

http://identifiers.org/hco/13/GRCh38#98249173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121370819-C-A

98249285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121370988-G-A

98249394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121371723-A-T

98249444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121371754-G-C

98249444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121371754-G-T

98249683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121371989-A-G

98249887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121372181-A-G

98250119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121372405-C-T

98250262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121372517-A-G

98250319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121372573-G-A

98250328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121372582-A-G

98252248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121374028-C-T

98252521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121374272-C-T

98252830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121374435-C-T

98253077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121374756-T-C

98253343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121374983-G-A

98253384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121375025-A-G

98253467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121375104-T-G

98253516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121375152-T-C

98253548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121375171-G-C

98253590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121375211-G-A

http://identifiers.org/hco/13/GRCh38#98253822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121375357-C-A

98253824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121375359-G-A

98254050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121375973-G-A

98254202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121376106-A-G

98254517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121376391-G-A

98254729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121376795-T-A

98254731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121376797-G-C

98254942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121377010-C-T

98255018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121377108-A-T

98255086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121377153-T-C

http://identifiers.org/hco/13/GRCh38#98255154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121377211-A-C

98260218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121380435-G-A

98260311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121380541-C-T

98265777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121382713-T-C

98265859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121382761-G-A

98266296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121383192-A-G

98266403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121383296-C-G

98266403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121383296-C-T

98266418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121383311-T-C

98266538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121383436-A-G

98267052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121383686-C-G

98267052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121383686-C-T

98267251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121383867-G-A

98267281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121383897-T-C

98267469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121384075-G-A

98267509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121384092-T-A

98267514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121384097-C-G

98267567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121384140-G-A

98267567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121384140-G-T

98267584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121384216-G-A

http://identifiers.org/hco/13/GRCh38#98267674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121384313-C-A

98267674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121384313-C-T

98267675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121384314-G-A

98267859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121384559-G-C

98267889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121384589-C-G

http://identifiers.org/hco/13/GRCh38#98267971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121384679-A-C

98267994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121384702-C-T

98268031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121384722-G-A

98268054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121384736-T-G

98270092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121385545-G-A

http://identifiers.org/hco/13/GRCh38#98270124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121385574-A-C

98270197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121385644-G-A

http://identifiers.org/hco/13/GRCh38#98270216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121385660-A-C

98270216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121385660-A-T

http://identifiers.org/hco/13/GRCh38#98270217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121385661-C-A

98270217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121385661-C-G

98270378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121385778-C-T

98270398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121385802-A-G

98270414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121385819-G-A

98270469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121386237-A-G

98270562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121386323-A-G

98270896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121386551-C-T

98270907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121386562-C-T

98271007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121386656-T-G

98274236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121388754-G-A

98274273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121388791-G-A

98274273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121388791-G-T

98274907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121389256-C-T

http://identifiers.org/hco/13/GRCh38#98275084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121389409-A-C

http://identifiers.org/hco/13/GRCh38#98275175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121389495-C-A

98275175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121389495-C-T

98275220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121389541-G-A

98275481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121390110-T-G

98275573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121390214-T-A

98275834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121390440-G-A

http://identifiers.org/hco/13/GRCh38#98275897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121390500-C-A

98275897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121390500-C-T

98275934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121390538-T-C

98276054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121390650-C-T

98276376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121390959-C-T

98276406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121390990-T-A

http://identifiers.org/hco/13/GRCh38#98276560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121391139-A-C

98279208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121393157-T-C

98280481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121396121-C-G

98280897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121396569-T-C

98281041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121396700-T-C

98281652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121397137-T-A

98281667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121397152-A-T

98281747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121397254-T-A

98281747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121397254-T-C

98282401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121397853-G-A

98282404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121397856-C-T

98282466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121397920-A-G

http://identifiers.org/hco/13/GRCh38#98282940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121398072-C-A

98282977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121398101-A-T

98282997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121398120-T-A

98283012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121398133-A-G

98283101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121398211-G-C

98283132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121398255-A-G

98283167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121398288-A-G

98283229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121398368-A-G

98283229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121398368-A-T

http://identifiers.org/hco/13/GRCh38#98283235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121398374-A-C

98283299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121398424-C-T

http://identifiers.org/hco/13/GRCh38#98283714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121398836-A-C

98283714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121398836-A-G

98283724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121398850-G-A

http://identifiers.org/hco/13/GRCh38#98284905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121400034-C-A

98285641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121401260-G-A

98285641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121401260-G-C

98285641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121401260-G-T

98285810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121401423-A-G

98285823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121401438-A-G

98285992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121401612-C-G

98286236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121401837-C-T

98288709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121402925-G-A

98288725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121402946-C-T

98288754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121402971-G-A

98288765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121402974-C-T

98288826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121403035-G-A

98289003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121403210-A-T

98289200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121403402-G-A

98289229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121403430-C-G

98289482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121403635-G-T

98289641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121403764-T-C

98289905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121404212-A-G

98290050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121404319-T-G

98290132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121404377-T-G

98291809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121405965-T-C

98291827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121405983-A-T

98292102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121406251-A-G

98292236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121406387-G-C

98292641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121407421-C-T

98292650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121407434-C-G

98292682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121407466-G-A

98292924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121407682-C-T

http://identifiers.org/hco/13/GRCh38#98292951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121407702-A-C

98293185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121407879-A-G

98293302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121407993-G-A

98293302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121407993-G-T

98293342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121408032-A-G

98293375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121408054-C-T

98293419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121408097-C-T

98293590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121408251-C-T

http://identifiers.org/hco/13/GRCh38#98293632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121408261-C-A

98293632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121408261-C-T

98293762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121408381-G-A

98293823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121408439-A-G

98293921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121408551-A-G

98295116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121408853-G-A

98295116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121408853-G-C

98295116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121408853-G-T

98295190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121408927-G-A

98295244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121408980-A-T

98295263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121409017-G-A

98295270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121409029-A-G

98295353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121409104-G-A

98295353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121409104-G-C

98295355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121409106-G-A

98295466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121409213-A-G

98295479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121409231-A-G

98295547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121409298-C-T

98296197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121409474-T-C

98296356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121409612-G-C

98296357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121409613-C-T

98296986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121409902-A-G

98296986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121409902-A-T

98297441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121410330-A-G

98298227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121411862-G-T

98298634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121412180-T-C

98298749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121412916-A-G

98298801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121412968-G-A

98299032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121413132-G-A

98299475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121413568-A-G

98300281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121413904-A-T

98300332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121413948-G-A

98300347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121413957-G-A

98300429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121414041-G-A

98300441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121414051-C-T

http://identifiers.org/hco/13/GRCh38#98300586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121414196-C-A

98300811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121414330-G-T

98300867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121414362-A-G

98300911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121414406-C-T

98300923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121414416-G-C

98301129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121414586-T-C

98301166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, undefined
orthologous variants: 121414615-G-A

98301335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121414777-G-A

98301385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121414792-C-T

98301390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121414796-A-G

98301418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121414822-A-G

http://identifiers.org/hco/13/GRCh38#98301433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121414837-C-A

98301732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121415369-C-T

98301872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121415516-T-C

98301946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121415592-G-A

98302177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121415807-G-C

98302266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121415878-A-G

http://identifiers.org/hco/13/GRCh38#98302321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121415928-C-A

98302321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121415928-C-G

98302397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121415984-A-G

98302501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121416098-C-T

98302696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121416256-T-A

98302741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121416290-G-A

98302741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121416290-G-T

98302762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121416299-T-A

98302978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121416486-C-T

98303038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121416534-T-C

98303075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121416580-T-C

98303092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121416596-G-A

98303092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121416596-G-T

98303361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121417479-A-G

http://identifiers.org/hco/13/GRCh38#98303368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121417486-C-A

98303368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121417486-C-T

98303373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121417491-G-A

98303742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121418024-G-C

98303772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121418054-T-A

http://identifiers.org/hco/13/GRCh38#98303836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121418116-A-C

98303934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121418220-C-T

98303976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121418261-C-T

98304112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121418380-C-G

98304112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121418380-C-T

98304184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121418431-C-T

98304254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121418497-T-G

http://identifiers.org/hco/13/GRCh38#98304334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121418551-C-A

98312782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121419512-C-T

98312787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121419517-G-A

98312800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121419531-C-G

98314731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121421250-G-C

98321226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121423058-G-A

98321245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121423077-G-A

98321275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121423108-G-A

98321477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121423277-A-T

http://identifiers.org/hco/13/GRCh38#98321546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121423345-A-C

98321588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121423373-G-T

98321633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121423420-G-C

98321659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121423443-C-T

http://identifiers.org/hco/13/GRCh38#98321882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121423639-C-A

98321903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121423662-C-T

98322850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121424581-T-C

98323716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121425868-A-G

98323892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121426041-C-T

http://identifiers.org/hco/13/GRCh38#98323937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121426085-C-A

98323952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121426100-T-G

98324024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121426167-A-G

98324117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121426466-A-G

98324232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121426664-G-T

98324291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121426723-A-G

98324305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121426737-A-G

98324521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121426923-G-C

98324565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121426963-A-G

98324714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427077-A-G

98324714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427077-A-T

http://identifiers.org/hco/13/GRCh38#98324816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121427178-C-A

98324816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427178-C-T

98324902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427346-G-A

98324911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427355-C-T

http://identifiers.org/hco/13/GRCh38#98324983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121427500-C-A

98325012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427529-C-T

http://identifiers.org/hco/13/GRCh38#98325013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121427530-A-C

98325013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427530-A-G

98325019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427536-G-T

98325208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427720-T-G

98325223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427733-T-G

98325250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427771-A-G

98325263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427784-T-C

98325353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427867-C-G

98325353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427867-C-T

98325425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427940-C-T

98325450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121427964-G-A

98325512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121428036-G-A

http://identifiers.org/hco/13/GRCh38#98325515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121428039-C-A

98325706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121428538-A-G

98325738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121428574-C-T

98325767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121428601-A-G

98325984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121428816-G-A

http://identifiers.org/hco/13/GRCh38#98326023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121428856-A-C

http://identifiers.org/hco/13/GRCh38#98326043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121428877-C-A

98326138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121428964-G-A

98326506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121429192-G-A

98326527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121429213-G-A

98326555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121429240-G-A

98326574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121429259-A-G

98326682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121429361-C-T

98327006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121429675-C-T

98327317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121430087-A-G

98327341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121430112-A-G

98329889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121431265-A-G

http://identifiers.org/hco/13/GRCh38#98329979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121431342-C-A

98329980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121431343-A-G

98329981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121431344-G-C

98329986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121431349-G-A

98329986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121431349-G-T

98329992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121431355-G-A

98329995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121431360-G-A

98329995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121431360-G-C

98329995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121431360-G-T

98330039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121431400-T-C

98330055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121431416-G-A

98330055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121431416-G-T

98330186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121431545-G-T

98331140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121432127-G-A

98331140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121432127-G-C

http://identifiers.org/hco/13/GRCh38#98331260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121432617-A-C

98331378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121432733-G-A

98331414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121432770-C-T

98331549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121432914-T-G

98331610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121432973-G-T

98331668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433019-A-G

98331757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433090-C-T

http://identifiers.org/hco/13/GRCh38#98331793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121433126-C-A

98331851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433172-A-G

98332067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433566-G-T

98332163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433637-C-G

98332163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433637-C-T

http://identifiers.org/hco/13/GRCh38#98332200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121433654-A-C

98332200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433654-A-G

http://identifiers.org/hco/13/GRCh38#98332225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121433679-C-A

98332225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433679-C-T

98332244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433693-T-A

98332244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433693-T-C

http://identifiers.org/hco/13/GRCh38#98332269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121433708-C-A

98332269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433708-C-T

98332293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433731-G-T

http://identifiers.org/hco/13/GRCh38#98332361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121433799-C-A

98332361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121433799-C-G

98332448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121433886-C-T

98332677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121435649-C-G

98332683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121435655-C-T

98332701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121435673-A-G

98332736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121435716-G-T

http://identifiers.org/hco/13/GRCh38#98332934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121435867-C-A

98332934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121435867-C-T

98332939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121435872-C-G

98332939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121435872-C-T

98332940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 121435873-G-A

98332940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 121435873-G-T

http://identifiers.org/hco/13/GRCh38#98333090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121436030-C-A

98333090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436030-C-T

98333103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436043-A-T

98333127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436065-G-T

98333192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436122-G-C

98333452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121436342-C-T

98333454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121436344-C-T

http://identifiers.org/hco/13/GRCh38#98333456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121436346-C-A

98333456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121436346-C-T

http://identifiers.org/hco/13/GRCh38#98333486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121436383-A-C

98333486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121436383-A-G

98333529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121436427-C-T

98333564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121436460-A-G

98333661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436555-G-C

98333751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436641-A-G

98333770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436659-G-A

98333770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436659-G-T

http://identifiers.org/hco/13/GRCh38#98333798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121436687-C-A

98333798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436687-C-T

98333865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436759-T-C

98333883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436777-G-A

http://identifiers.org/hco/13/GRCh38#98333938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121436816-C-A

98333938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436816-C-T

98333954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436827-T-A

98333954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436827-T-G

http://identifiers.org/hco/13/GRCh38#98333959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121436832-C-A

98333959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436832-C-G

http://identifiers.org/hco/13/GRCh38#98333985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121436859-A-C

98334086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436948-T-C

98334210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121437059-T-C

98334211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121437060-G-T

98334213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121437062-A-G

98334223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121437072-G-A

98334223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121437072-G-T

98334227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121437076-A-G

98334227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121437076-A-T

http://identifiers.org/hco/13/GRCh38#98334229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121437078-C-A

98335109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121440817-G-T

98335123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121440831-C-G

98336756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121441085-G-A

98336781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121441110-A-G

98337059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121441385-T-A

98339523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121442506-C-T

98339532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121442515-T-C

http://identifiers.org/hco/13/GRCh38#98339839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121442813-C-A

98339903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121442874-G-T

98339946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121442921-G-A

98339946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121442921-G-C

http://identifiers.org/hco/13/GRCh38#98340004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121442968-A-C

98340364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121443324-A-G

98340680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121443395-G-A

98340691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121443406-T-C

98340878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121443580-G-T

98340937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121443639-A-G

98340955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121443650-A-G

98341119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121443813-T-C

98341133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121443827-G-T

98341134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121443828-C-T

98341149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121443843-A-G

98341153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121443847-A-G

98341158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121443852-T-G

98341257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121443945-A-T

98343694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121444600-G-T

http://identifiers.org/hco/13/GRCh38#98343719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121444617-C-A

98343719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121444617-C-G

98343719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121444617-C-T

http://identifiers.org/hco/13/GRCh38#98343720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121444618-C-A

98343720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121444618-C-T

http://identifiers.org/hco/13/GRCh38#98343794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121444698-A-C

98343815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121444719-C-G

98343815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121444719-C-T

98343837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121444741-C-T

http://identifiers.org/hco/13/GRCh38#98343890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121444806-A-C

98343890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121444806-A-G

98343890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121444806-A-T

98343949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121444860-G-A

98343949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121444860-G-C

98343949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121444860-G-T

98344858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121445967-C-T

98344914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121446007-C-T

98345025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121446102-T-G

98345122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121446179-C-G

98345281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121446336-T-A

98345386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121446417-A-G

98345398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121446433-T-C

98346751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121447085-A-G

98346771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121447105-G-T

98346793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121447127-G-A

http://identifiers.org/hco/13/GRCh38#98346930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121447269-C-A

98346930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121447269-C-T

98347043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121447393-G-A

98347213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121447697-A-G

98347245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121447731-G-A

98347661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121448055-G-A

98347867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121448208-T-C

98348226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121448580-T-C

98348229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121448583-C-T

http://identifiers.org/hco/13/GRCh38#98349701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121450871-A-C

98349703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121450873-G-A

98349703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121450873-G-C

98349703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121450873-G-T

98349704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121450874-A-G

98349708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121450878-T-A

98349708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121450878-T-G

98349731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121450900-A-G

98349825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121450983-T-A

98349960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121451085-G-A

98350047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121451168-T-G

98350165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121451261-G-A

98353886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121451385-A-G

98353913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121451410-T-C

98353981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121451478-T-C

98354121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121451946-C-G

98354179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121452005-C-T

98354460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121452243-A-G

98354481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121452264-T-C

http://identifiers.org/hco/13/GRCh38#98354567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121452350-C-A

98364122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121454836-G-C

98364387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121455127-G-C

98364389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121455129-T-G

98364391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121455130-G-A

98364391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121455130-G-T

98364440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121455179-T-A

98364450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121455189-C-T

98364777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121455468-G-A

98364920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121455593-T-C

98364932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121455604-A-T

98365014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121455714-A-G

98365040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121455759-G-T

98365082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121455814-A-G

98365141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121455881-T-C

98365141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121455881-T-G

http://identifiers.org/hco/13/GRCh38#98365280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121456691-C-A

98365280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121456691-C-G

98365280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121456691-C-T

98365397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 121456791-G-A

98365465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121456859-G-A

98365465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121456859-G-T

http://identifiers.org/hco/13/GRCh38#98365512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121456907-C-A

98365512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121456907-C-G

98365642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121457039-C-T

98365872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121457783-G-A

98365872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121457783-G-T

98365877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121457788-A-T

98366277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121458157-G-A

98366413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121458235-A-G

98366672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121458417-T-G

98368217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121460150-T-A

98368217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121460150-T-C

98368280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121460207-A-G

98368330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121460257-A-T

98368458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121460385-C-T

98371506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121462030-A-G

98371670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121462182-G-T

98371695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121462207-C-T

98371791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121462447-C-T

98372595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121463112-G-A

98372748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121463269-G-A

98372909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121463340-C-T

98373185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121463581-C-T

98373196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121463592-G-T

98373338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121463722-T-C

98373360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121463753-C-T

98373397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121463780-T-C

http://identifiers.org/hco/13/GRCh38#98373501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121463897-C-A

98373555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121463951-C-G

98373564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121463960-A-G

98374043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121465380-C-T

http://identifiers.org/hco/13/GRCh38#98377712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121467912-C-A

http://identifiers.org/hco/13/GRCh38#98377734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121467933-C-A

98377734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121467933-C-T

98377747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121467946-T-C

http://identifiers.org/hco/13/GRCh38#98377792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121468012-C-A

98377792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121468012-C-G

98377792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121468012-C-T

http://identifiers.org/hco/13/GRCh38#98377816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121468036-C-A

98377816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121468036-C-G

98377816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121468036-C-T

http://identifiers.org/hco/13/GRCh38#98377908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121468128-C-A

98377946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121468166-T-C

98378026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121468229-G-A

98378026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121468229-G-C

98378046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121468249-G-A

98383286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121469563-A-G

98383444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121469683-G-T

98383461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121469700-A-G

98383476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121469719-G-T

98383520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121469755-C-T

98383523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121469759-G-T

http://identifiers.org/hco/13/GRCh38#98383535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121469771-C-A

98383732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121469936-A-G

98383743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121469947-G-T

98383801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121470004-G-T

98383871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121470080-C-T

98384453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121470873-A-G

http://identifiers.org/hco/13/GRCh38#98384486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121470902-C-A

98384486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121470902-C-T

98384497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121470908-A-G

http://identifiers.org/hco/13/GRCh38#98384552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121470962-C-A

98384589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121471000-A-G

98384702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121471107-A-G

98384702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121471107-A-T

98384704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121471116-C-T

98384705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121471117-T-C

98384714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121471126-T-C

98384714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121471126-T-G

98384740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121471152-G-C

98384806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121471218-A-G

98384843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: coding_sequence_variant, incomplete_terminal_codon_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 121471255-A-G

http://identifiers.org/hco/13/GRCh38#98384881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121471293-C-A

98384881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121471293-C-T

http://identifiers.org/hco/13/GRCh38#98384929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121471734-C-A

98384929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121471734-C-G

98384929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121471734-C-T

http://identifiers.org/hco/13/GRCh38#98384933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121471738-C-A

98384933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121471738-C-T

98384977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121471785-A-G

98385035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121471855-A-G

98385138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121471956-G-A

98385167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121471984-C-T

http://identifiers.org/hco/13/GRCh38#98385395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121472231-C-A

98385395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121472231-C-G

98385562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121472374-G-A

98385562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121472374-G-T

98385587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121472398-G-A

98385587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121472398-G-T

98385848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121472653-G-C

98385874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121472747-T-A

98385874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121472747-T-C

98385890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121472763-A-G

98385935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121472814-G-T

98385947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121472826-T-A

98385947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121472826-T-C

http://identifiers.org/hco/13/GRCh38#98385967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121472858-C-A

98385967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121472858-C-T

98386038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121472920-G-C

http://identifiers.org/hco/13/GRCh38#98386072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121472955-C-A

98386072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121472955-C-T

98386107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121472990-G-A

98386107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121472990-G-T

98386156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121473038-C-T

98386168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121473055-A-T

98386185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121473072-T-C

98386884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121473707-G-A

http://identifiers.org/hco/13/GRCh38#98386924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121473749-C-A

98387455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121473978-T-C

98387943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121474155-G-A

98387943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121474155-G-T

98388022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121474231-A-G

98388152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121474355-C-G

98388152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121474355-C-T

98388292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121474482-C-G

98388335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121474501-T-C

98388445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121474610-G-A

http://identifiers.org/hco/13/GRCh38#98388507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121474665-C-A

98388507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121474665-C-G

98388507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121474665-C-T

98388509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121474667-T-C

98388535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121474691-G-A

98388541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121474697-G-A

98388541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121474697-G-C

98388543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121474699-T-G

98388550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121474707-C-T

98388681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121474811-C-G

http://identifiers.org/hco/13/GRCh38#98388847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121474973-C-A

98388848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121474974-A-G

98388880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475006-C-G

98388880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475006-C-T

98389100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475196-A-T

98389185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475263-C-T

98389187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475273-A-G

98389201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475287-T-C

98389328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475410-T-C

98389365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475447-G-A

98389365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475447-G-C

98389365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475447-G-T

98389377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475459-G-T

98389391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475480-T-C

98389488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121475580-T-A

98389488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121475580-T-C

98389488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121475580-T-G

98389489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121475581-G-A

98389489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121475581-G-C

98389489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121475581-G-T

http://identifiers.org/hco/13/GRCh38#98389504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121475596-C-A

98389509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121475601-G-T

98389522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121475614-T-C

98389541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121475637-G-A

98389541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121475637-G-C

98389563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121475659-T-A

98389563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121475659-T-G

98389564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121475660-G-T

98389566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121475662-G-T

http://identifiers.org/hco/13/GRCh38#98389705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121475803-C-A

98389705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475803-C-T

http://identifiers.org/hco/13/GRCh38#98389849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121475885-C-A

98389849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475885-C-G

98389849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121475885-C-T

http://identifiers.org/hco/13/GRCh38#98389875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121475911-C-A

98389959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 121476042-T-C

98389959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 121476042-T-G

http://identifiers.org/hco/13/GRCh38#98390013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121476096-C-A

98390013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: synonymous variant
orthologous variants: 121476096-C-T

98390028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: synonymous variant
orthologous variants: 121476111-T-C

98390067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: synonymous variant
orthologous variants: 121476150-C-T

http://identifiers.org/hco/13/GRCh38#98390166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121476258-C-A

98390193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121476284-A-T

http://identifiers.org/hco/13/GRCh38#98390209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121476300-A-C

98390209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121476300-A-G

98390249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121476331-G-A

98390250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121476332-G-A

98390250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121476332-G-T

http://identifiers.org/hco/13/GRCh38#98390260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121476342-A-C

98390260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121476342-A-G

http://identifiers.org/hco/13/GRCh38#98390270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121476352-C-A

98390438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121477064-G-T

98390468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121477094-T-G

98390469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121477099-G-T

98390478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121477108-G-A

98390478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121477108-G-T

98390527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121477163-A-T

http://identifiers.org/hco/13/GRCh38#98390528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121477164-A-C

98390532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121477168-C-T

98390580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121477221-G-A

98390580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121477221-G-T

98390594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121477235-G-C

98390594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121477235-G-T

98390613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121477255-T-G

http://identifiers.org/hco/13/GRCh38#98390658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121477301-C-A

98390768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121477342-T-C

98390799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121477373-G-A

98390799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121477373-G-T

http://identifiers.org/hco/13/GRCh38#98390894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121477466-C-A

98390900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121477472-T-A

98390900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121477472-T-C

98390901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121477473-A-G

98390920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121477489-T-C

98390957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121477494-T-C

98390972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121477507-T-C

http://identifiers.org/hco/13/GRCh38#98390978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121477513-C-A

98392857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479183-C-T

98393083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479354-G-A

98393209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479456-A-G

98393432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479638-C-T

98393453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479659-A-G

98393483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479681-G-A

98393483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479681-G-T

98393519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479716-G-A

98393519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479716-G-T

98393525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479722-A-G

http://identifiers.org/hco/13/GRCh38#98393605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121479762-C-A

98393605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479762-C-G

98393731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479887-G-A

98393731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479887-G-T

http://identifiers.org/hco/13/GRCh38#98393751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121479901-C-A

98393751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479901-C-T

98393768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479914-T-C

98393768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479914-T-G

98393795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479942-G-C

98393795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479942-G-T

http://identifiers.org/hco/13/GRCh38#98393847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121479987-A-C

98393847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479987-A-T

98393852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479992-G-A

98393854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479994-G-A

98393854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479994-G-C

98393854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479994-G-T

98394127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121480135-G-T

98394490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121480481-G-A

98394504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121480495-T-C

98395196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121480746-C-G

http://identifiers.org/hco/13/GRCh38#98395238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121480776-C-A

98395276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121480814-G-A

98395277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121480815-G-A

98395403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121480941-C-T

http://identifiers.org/hco/13/GRCh38#98395439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121480983-C-A

http://identifiers.org/hco/13/GRCh38#98395532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/14/GRCm39#121481076-C-A

98395532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481076-C-G

98395532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121481076-C-T

98395662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481188-A-G

98395716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481242-T-A

98395716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481242-T-C

98395716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481242-T-G

http://identifiers.org/hco/13/GRCh38#98395743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121481269-C-A

98395743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481269-C-G

98395743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481269-C-T

98395757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121481283-A-G

98395790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121481316-T-A

98395790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121481316-T-C

98395790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121481316-T-G

98395838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121481364-G-A

98395838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121481364-G-T

98395859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121481385-C-T

98396023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481549-C-T

http://identifiers.org/hco/13/GRCh38#98396096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121481622-C-A

98396096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481622-C-G

98396096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121481622-C-T

http://identifiers.org/hco/13/GRCh38#98396200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121481732-C-A

98396212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481744-G-A

98396212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481744-G-C

98396257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481789-G-A

98396257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481789-G-T

98396342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481877-G-T

http://identifiers.org/hco/13/GRCh38#98396383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121481918-C-A

98396389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, missense_variant
orthologous variants: 121481924-T-C

http://identifiers.org/hco/13/GRCh38#98396432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121481967-C-A

98396432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 121481967-C-T

http://identifiers.org/hco/13/GRCh38#98396524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121482038-C-A

98396526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121482040-T-C

98396527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121482041-G-T

98396762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121482269-G-A

98396762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121482269-G-T

98396787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121482286-A-G

98396798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121482297-G-A

98396798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121482297-G-T

98396803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121482302-T-C

98396885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121482367-G-T

98396959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121482437-C-G

98397069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121482545-G-A

98397165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121482632-G-A

98397364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121482796-G-A

98397509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121482883-T-C

98397710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121483071-G-A

98397711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121483072-G-A

98397711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121483072-G-T

98397830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121483203-C-T

http://identifiers.org/hco/13/GRCh38#98398005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121483328-C-A

98398005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121483328-C-T

98398068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121483389-G-T

98398218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121483507-T-G

98398245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121483530-A-G

98398409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121483671-A-G

http://identifiers.org/hco/13/GRCh38#98398422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121483689-C-A

98398670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121483900-C-T

98398744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121483977-T-C

98398862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121484087-G-A

98399196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121484306-T-C

98399222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121484331-G-T

98399281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121484387-G-A

98399281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121484387-G-T

98399301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121484407-T-C

98399524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121484613-G-T

98399632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121484688-G-A

98399637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121484693-G-T

98399713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121484764-A-G

98399789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121484832-G-A

98399811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121484854-T-C

98399861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121484890-G-A

98399861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121484890-G-T

http://identifiers.org/hco/13/GRCh38#98400042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121485071-C-A

98400172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121485219-T-C

http://identifiers.org/hco/13/GRCh38#98400215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121485272-C-A

98400347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121485364-G-C

98400518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121485549-G-A

98400528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121485559-G-C

http://identifiers.org/hco/13/GRCh38#98400627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121485644-C-A

98400627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121485644-C-G

98400640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121485657-C-T

98400976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121485861-T-C

98401329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486062-G-T

http://identifiers.org/hco/13/GRCh38#98401423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121486170-C-A

98401423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486170-C-T

98401433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486180-C-G

98401486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486226-G-A

98401486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486226-G-T

http://identifiers.org/hco/13/GRCh38#98401490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121486230-C-A

98401490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486230-C-T

98401496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486236-G-T

98401555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486285-G-A

98401573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486303-T-A

98401645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486374-G-A

98401662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486390-G-A

98401662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486390-G-T

98401678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486401-A-G

http://identifiers.org/hco/13/GRCh38#98401683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121486406-C-A

98401714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486465-T-A

98401714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486465-T-G

http://identifiers.org/hco/13/GRCh38#98401719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121486470-C-A

http://identifiers.org/hco/13/GRCh38#98401761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121486496-C-A

http://identifiers.org/hco/13/GRCh38#98401906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121486641-C-A

98401906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486641-C-T

98401940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486675-G-T

98401945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486680-G-T

98402012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486752-A-G

98402102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486810-C-T

http://identifiers.org/hco/13/GRCh38#98402125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121486833-A-C

98402142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486850-T-C

98402169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486877-A-G

98402270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486940-G-T

98402373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121486964-T-C

98402529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487023-T-A

98402542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487036-A-G

98402553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487047-T-C

98402630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487112-A-G

98402814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487288-C-T

http://identifiers.org/hco/13/GRCh38#98402856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121487333-A-C

98402889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487367-A-G

98403004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487481-C-G

98403004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487481-C-T

http://identifiers.org/hco/13/GRCh38#98403104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121487579-C-A

98403104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487579-C-G

98403104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487579-C-T

http://identifiers.org/hco/13/GRCh38#98403180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121487632-C-A

http://identifiers.org/hco/13/GRCh38#98403229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121487670-C-A

98403301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487749-A-G

98403301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487749-A-T

98403309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487757-A-G

98403332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487780-G-T

98403373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487820-G-A

98403394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487841-A-T

98403417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487864-A-G

http://identifiers.org/hco/13/GRCh38#98403477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121487906-C-A

98403519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121487909-G-A

http://identifiers.org/hco/13/GRCh38#98403694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121488040-A-C

98403694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121488040-A-G

98403701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121488047-A-T

98403730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121488077-G-A

98403730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121488077-G-C

98403738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121488085-T-C

98403927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121488281-G-A

98403927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121488281-G-T

98403993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121488328-T-C

98403994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121488329-G-A

98403994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121488329-G-C

98403994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121488329-G-T

98404160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121488476-T-C

98404164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121488480-C-T

98404188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121488506-T-C

http://identifiers.org/hco/13/GRCh38#98404271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121488589-C-A

98404274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121488592-A-G

98404318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121488636-C-T

98404386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121488695-G-A

98404386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121488695-G-T

http://identifiers.org/hco/13/GRCh38#98404413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121488717-C-A

98404511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121488782-G-A

98404511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121488782-G-T

98404674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121488940-A-G

98404745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121489000-G-A

98404962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121489166-A-G

98405155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121489389-G-T

98405178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121489400-T-C

98405445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121489661-G-T

http://identifiers.org/hco/13/GRCh38#98405584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121489738-C-A

98405584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121489738-C-T

http://identifiers.org/hco/13/GRCh38#98405725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121489854-C-A

98405800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121489936-C-T

98405811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121489947-A-G

98405811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121489947-A-T

98405815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121489951-G-T

98406022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490078-C-T

98406058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490103-C-G

98406058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490103-C-T

98406236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490216-G-A

98406382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490320-A-G

http://identifiers.org/hco/13/GRCh38#98406385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121490323-C-A

98406410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490348-A-G

98406419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490356-G-T

98406520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490449-G-T

http://identifiers.org/hco/13/GRCh38#98406540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121490468-C-A

98406563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490490-T-C

98406585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490506-G-A

98406585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490506-G-T

98406712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490605-T-C

http://identifiers.org/hco/13/GRCh38#98406758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121490635-C-A

98406758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490635-C-G

98406772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490649-G-A

98406809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490694-G-A

98406809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490694-G-T

98406831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490719-A-G

98406842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490730-C-T

98406874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490782-A-G

98406897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490805-G-T

98407009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121490911-T-C

98407208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121491097-A-G

98407218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121491108-G-A

98407355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121491245-T-C

98407357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121491247-T-A

98407357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121491247-T-C

98407993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121491834-T-C

98407997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121491838-T-C

98408012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121491854-G-A

98408023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121491865-C-G

98408218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492006-T-C

98408321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492101-A-T

98408822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492300-C-G

98408822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492300-C-T

98408923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492400-G-A

98409232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492713-G-A

98409232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492713-G-T

98409233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492714-G-A

98409233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492714-G-T

98409260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492741-G-A

98409260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492741-G-T

98409396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121492878-G-A

98409408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121492890-C-T

98409468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121492950-G-A

98409468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121492950-G-C

98409468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121492950-G-T

98409486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121492968-C-T

98409498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121492980-G-A

98409628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121493052-T-C

98409631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121493055-G-T

98409703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121493066-A-G

98409708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121493071-C-T

98410136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121493412-G-T

http://identifiers.org/hco/13/GRCh38#98410183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121493462-A-C

98410247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121493521-G-T

98410378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121493645-G-A

98410403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121493683-C-T

98410643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494025-G-A

http://identifiers.org/hco/13/GRCh38#98410688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121494085-C-A

98410793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121494188-A-G

http://identifiers.org/hco/13/GRCh38#98410831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121494226-C-A

98410831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121494226-C-G

98410831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121494226-C-T

98410833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494228-G-A

http://identifiers.org/hco/13/GRCh38#98410841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121494242-C-A

98410841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494242-C-T

http://identifiers.org/hco/13/GRCh38#98410842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121494243-C-A

98410842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494243-C-T

http://identifiers.org/hco/13/GRCh38#98410849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121494250-A-C

98410849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494250-A-G

98410860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494255-T-C

98410867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494262-T-A

98410892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494288-G-A

98410892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494288-G-T

http://identifiers.org/hco/13/GRCh38#98410923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121494319-C-A

98410923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494319-C-T

98410959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494362-A-T

98411023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494423-A-G

98411155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494552-C-T

98411435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494774-C-T

98411567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494870-T-A

98411572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494875-A-G

98411605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494908-A-G

98411605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494908-A-T

98411687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494987-C-G

98411752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495048-G-A

98411752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495048-G-C

98411753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495049-G-A

98411753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495049-G-T

98411774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495073-G-A

98411774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495073-G-T

98411776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495075-C-T

http://identifiers.org/hco/13/GRCh38#98411782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121495081-C-A

http://identifiers.org/hco/13/GRCh38#98411787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121495086-C-A

98411788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495087-A-G

http://identifiers.org/hco/13/GRCh38#98411808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121495115-C-A

98411808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495115-C-T

98411890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495234-C-T

98411966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121495310-G-A

98412061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495410-C-T

98412079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495434-G-T

98412179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495510-C-T

98412189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495520-C-T

98412551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496394-A-G

98412741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496607-A-G

98412788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496659-A-G

98412914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496795-T-G

98413205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497047-G-T

98415736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498287-C-T

98416278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499385-T-C

98416331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499423-T-C

98416339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121499431-G-A

98416339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121499431-G-C

98416339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121499431-G-T

http://identifiers.org/hco/13/GRCh38#98416538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#121499608-A-C

http://identifiers.org/hco/13/GRCh38#98416542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#121499612-C-A

98416542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121499612-C-T

98420383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121501508-C-T

http://identifiers.org/hco/13/GRCh38#98420408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121501533-A-C

98420545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121501679-C-T

98420563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121501697-G-A

98420563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121501697-G-T

98420590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121501724-C-T

http://identifiers.org/hco/13/GRCh38#98420755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121501849-A-C

98420865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121501958-G-A

98420922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121501987-G-C

98421072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121502103-G-T

98421118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121502139-G-C

http://identifiers.org/hco/13/GRCh38#98421147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121502168-C-A

http://identifiers.org/hco/13/GRCh38#98424436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121505162-C-A

98424436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121505162-C-G

98424467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121505204-G-A

98424467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121505204-G-T

98424474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121505211-G-A

98424474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121505211-G-T

98424500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121505237-G-C

98424500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121505237-G-T

98424603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121505319-T-C

98424603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121505319-T-G

98425726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121505561-A-G

98425900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121505697-C-T

98426027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121505820-C-T

98427348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121507860-T-C

98427373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121507885-C-T

98427485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121507963-G-A

98427550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121508022-C-T

http://identifiers.org/hco/13/GRCh38#98427752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121508206-C-A

98427752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121508206-C-G

98430807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121508900-A-G

98430837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121508930-A-G

98430971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121509035-A-G

98430981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121509041-G-A

98430981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121509041-G-T

98431006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121509058-A-G

http://identifiers.org/hco/13/GRCh38#98431019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121509073-C-A

98431024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121509078-T-A

98431112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: missense variant
orthologous variants: 121509161-C-T

98431294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121509342-G-A

98431294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121509342-G-T

98431319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121509354-A-G

http://identifiers.org/hco/13/GRCh38#98431352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121509373-A-C

98431352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121509373-A-G

98431352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121509373-A-T

98431374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121509389-G-A

98431374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121509389-G-T

http://identifiers.org/hco/13/GRCh38#98431411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121509420-C-A

98431411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121509420-C-G

98431411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121509420-C-T

98433899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121509675-G-T

98433938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121509710-C-T

98434013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121509763-T-C

98434097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121509843-G-A

98434127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121509871-G-T

http://identifiers.org/hco/13/GRCh38#98434205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121509932-C-A

98434210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121509937-G-A

98434210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121509937-G-T

http://identifiers.org/hco/13/GRCh38#98434287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121509994-C-A

98434287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121509994-C-T

98434295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121510002-G-A

98434304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121510011-A-G

98434362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121510051-G-A

98434380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121510071-G-A

98434390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121510081-A-G

http://identifiers.org/hco/13/GRCh38#98435616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121510196-C-A

98435616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121510196-C-T

98435619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121510199-T-C

98438122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121512386-A-T

98438272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121512530-A-G

98438897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121512881-T-G

98438935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121512913-A-T

98438936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121512914-G-A

98438941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121512919-G-T

98439145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: synonymous variant
orthologous variants: 121513036-G-A

http://identifiers.org/hco/13/GRCh38#98439169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121513060-C-A

98439169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: synonymous variant
orthologous variants: 121513060-C-T

98439248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121513101-G-T

http://identifiers.org/hco/13/GRCh38#98439341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121513125-A-C

98439341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121513125-A-G

98439341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121513125-A-T

98439430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121513176-C-G

98439745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121513436-G-C

98439785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121513470-G-A

http://identifiers.org/hco/13/GRCh38#98439858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121513540-C-A

98439904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121513579-G-A

98439904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121513579-G-T

98439911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121513586-T-G

http://identifiers.org/hco/13/GRCh38#98439932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121513619-A-C

98439932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121513619-A-G

98440009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: missense variant
orthologous variants: 121513697-C-T

98440346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121514001-T-C

http://identifiers.org/hco/13/GRCh38#98440367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121514015-A-C

98440367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121514015-A-G

98440420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121514033-G-T

98440425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121514038-G-A

98440478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121514111-G-A

98440509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121514156-T-C

98440515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121514161-G-A

98440526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121514168-T-C

98440602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121514255-T-C

98440624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121514266-G-A

98440624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121514266-G-T

98440692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: synonymous variant
orthologous variants: 121514333-G-A

98440722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: synonymous variant
orthologous variants: 121514363-C-T

98440743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: synonymous variant
orthologous variants: 121514384-G-A

98441995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121515018-G-A

98441995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121515018-G-T

98442031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121515053-C-G

98442156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121515172-C-G

98442156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121515172-C-T

98442224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121515244-C-T

98442475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: intron variant
orthologous variants: 121515448-G-A

98445190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516351-G-A

98445246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516403-G-A

98445246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516403-G-C

98445246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516403-G-T

98445262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121516418-A-T

98445307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516469-A-T

98445379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516546-G-C

http://identifiers.org/hco/13/GRCh38#98445397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121516567-C-A

98445397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516567-C-T

http://identifiers.org/hco/13/GRCh38#98445423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#121516594-C-A

http://identifiers.org/hco/13/GRCh38#98445428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#121516599-C-A

98445428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121516599-C-G

98445428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121516599-C-T

http://identifiers.org/hco/13/GRCh38#98445486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#121516664-C-A

98445486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121516664-C-T

98445503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121516683-C-T

http://identifiers.org/hco/13/GRCh38#98445558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#121516742-C-A

98445558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121516742-C-G

98445558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121516742-C-T

98445568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121516752-G-A

98445568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121516752-G-T

98445616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121516791-T-C

98445616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121516791-T-G

http://identifiers.org/hco/13/GRCh38#98445665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#121516836-C-A

98445665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121516836-C-T

http://identifiers.org/hco/13/GRCh38#98445695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121516869-C-A

98445695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516869-C-G

98445695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516869-C-T

http://identifiers.org/hco/13/GRCh38#98445735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#121516893-C-A

98445735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121516893-C-T

98445771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516930-G-A

98445771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516930-G-C

98445771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516930-G-T

98445772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516931-T-A

98445772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516931-T-C

98445772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516931-T-G

98445838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121516975-T-G

98445920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121517076-G-A

98445920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121517076-G-T

98446022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121517180-T-C

98446039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121517191-T-C

http://identifiers.org/hco/13/GRCh38#98446040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121517192-C-A

98446040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121517192-C-T

98446052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121517202-G-A

98446052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121517202-G-T

http://identifiers.org/hco/13/GRCh38#98446082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121517227-C-A

98446082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121517227-C-G

98446082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121517227-C-T

http://identifiers.org/hco/13/GRCh38#98446083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121517228-C-A

98446083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121517228-C-G

98446083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121517228-C-T

http://identifiers.org/hco/13/GRCh38#98446233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121517385-C-A

98446233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121517385-C-T

98446663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 121518229-C-T

98446719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121518285-C-T

98446722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121518288-T-C

98446722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121518288-T-G

98446829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121518395-C-G

http://identifiers.org/hco/13/GRCh38#98446866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121518435-C-A

http://identifiers.org/hco/13/GRCh38#98446869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121518438-C-A

98446869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121518438-C-G

98448221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121519706-G-A

98448221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121519706-G-T

http://identifiers.org/hco/13/GRCh38#98448330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121519816-C-A

98448330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121519816-C-G

http://identifiers.org/hco/13/GRCh38#98448349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121519842-C-A

98448404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121519880-A-G

98448417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121519895-T-A

98448464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121519956-T-C

98448465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121519957-T-C

http://identifiers.org/hco/13/GRCh38#98448476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121519968-C-A

98448476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121519968-C-T

98448555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121520053-G-A

http://identifiers.org/hco/13/GRCh38#98448627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121520120-C-A

98448627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121520120-C-T

http://identifiers.org/hco/13/GRCh38#98448629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121520122-C-A

98448629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121520122-C-G

98448869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121520282-A-G

98448900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121520313-T-G

http://identifiers.org/hco/13/GRCh38#98448912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121520325-C-A

98448912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121520325-C-T

98448945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121520357-T-A

98448967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121520379-C-T

http://identifiers.org/hco/13/GRCh38#98449053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121520460-C-A

98449053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121520460-C-T

98449156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121520558-A-G

98449160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121520562-G-T

98449241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121520638-T-C

98449443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121520868-G-C

98449443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121520868-G-T

http://identifiers.org/hco/13/GRCh38#98449458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121520883-C-A

98449458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121520883-C-T

98449592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121520998-T-C

98449592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121520998-T-G

http://identifiers.org/hco/13/GRCh38#98449770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121521157-C-A

http://identifiers.org/hco/13/GRCh38#98449796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121521174-C-A

98449796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521174-C-T

98449835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521219-G-T

98449846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521235-G-A

98449846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521235-G-C

98449846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521235-G-T

98450016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521410-T-C

http://identifiers.org/hco/13/GRCh38#98450104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121521505-C-A

http://identifiers.org/hco/13/GRCh38#98450176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121521586-C-A

http://identifiers.org/hco/13/GRCh38#98450242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121521638-C-A

http://identifiers.org/hco/13/GRCh38#98450300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121521678-C-A

http://identifiers.org/hco/13/GRCh38#98450512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121521833-C-A

98450532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521859-T-C

98450538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521865-G-A

98450538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521865-G-C

98450538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521865-G-T

http://identifiers.org/hco/13/GRCh38#98450546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121521873-C-A

98450546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521873-C-T

http://identifiers.org/hco/13/GRCh38#98450553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121521880-A-C

98450553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521880-A-G

98450555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521882-A-G

98450556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521883-G-A

98450556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121521883-G-T

98450714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522115-G-A

98450714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522115-G-T

http://identifiers.org/hco/13/GRCh38#98450814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121522207-C-A

98450814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522207-C-G

98450814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522207-C-T

98450909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522303-G-A

98450909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522303-G-T

98450919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522313-T-C

98450962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522351-C-T

98450995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522385-A-G

98451007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522397-G-A

98451007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522397-G-T

98451010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522400-G-C

98451010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522400-G-T

98451035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522426-G-A

98451035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522426-G-T

98451046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121522441-T-C

http://identifiers.org/hco/13/GRCh38#98451166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121522652-C-A

98451455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121523103-T-C

98451591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121523236-T-G

98451628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121523271-A-G

98451628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121523271-A-T

98451635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121523278-C-T

98451661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121523300-T-A

98451705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121523336-G-T

98451869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121523468-G-A

98451869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121523468-G-C

98451869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121523468-G-T

http://identifiers.org/hco/13/GRCh38#98451981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121523578-C-A

98451981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121523578-C-T

98452056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121523653-G-A

98452477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121524057-C-T

98452594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121524178-T-C

98452828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121524412-T-C

http://identifiers.org/hco/13/GRCh38#98452954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121524526-C-A

98452954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121524526-C-T

98453027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121524595-G-A

98453027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121524595-G-C

98453027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121524595-G-T

98453051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121524627-G-A

98453051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121524627-G-C

98453051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3 prime UTR variant
orthologous variants: 121524627-G-T

98453262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121524817-G-A

98453262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121524817-G-T

98453265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121524820-A-G

http://identifiers.org/hco/13/GRCh38#98453297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#121524838-C-A

98453297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121524838-C-T

98454634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121526739-G-C

98454634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3591
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 121526739-G-T