http://identifiers.org/hco/1/GRCh38#222712571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
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/1/GRCm39#183078809-C-A

222712571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078809-C-G

222712571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078809-C-T

http://identifiers.org/hco/1/GRCh38#222712625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183078765-A-C

222712660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183078730-T-A

222712728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183078662-C-T

222712729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183078661-C-T

222712737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183078653-T-C

222712737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183078653-T-G

222712765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078625-G-A

222712765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078625-G-C

222712765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078625-G-T

222712768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078622-T-A

222712768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078622-T-C

222712768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078622-T-G

http://identifiers.org/hco/1/GRCh38#222712799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
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/1/GRCm39#183078592-A-C

222712799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078592-A-G

222712799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078592-A-T

222712808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078583-T-C

222712808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078583-T-G

222712809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078582-G-T

222712879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078511-G-A

222712879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078511-G-T

222712958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078427-G-A

222712958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078427-G-T

222712974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183078415-T-A

222712989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183078400-C-T

http://identifiers.org/hco/1/GRCh38#222713016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#183078374-C-A

222713016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078374-C-T

222713152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078300-G-A

222713203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078250-G-A

222713203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078250-G-T

222713308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078161-G-A

222713316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078154-G-A

222713316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078154-G-T

222713337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078133-T-C

222713353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078122-A-G

222713353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078122-A-T

http://identifiers.org/hco/1/GRCh38#222713367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#183078108-C-A

222713367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078108-C-T

222713435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078047-T-G

222713460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 183078018-T-G

222713473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183078005-G-A

http://identifiers.org/hco/1/GRCh38#222713512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#183077966-C-A

222714110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076885-C-G

222714110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076885-C-T

222714132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076865-G-T

222714169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076828-C-G

222714229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076763-T-C

222714236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076756-G-T

222714237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076755-A-G

222714237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076755-A-T

222714883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076685-T-A

222715011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076563-G-A

http://identifiers.org/hco/1/GRCh38#222715013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183076561-C-A

222715162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183076409-A-G

222715351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076212-T-C

222715374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076199-T-A

222715604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076085-A-G

222715611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076076-G-C

222715611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076076-G-T

222715633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076055-T-C

222715668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183076028-A-T

222715683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 183076013-G-C

222715683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 183076013-G-T

222715835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183075852-G-A

http://identifiers.org/hco/1/GRCh38#222715887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183075795-A-C

http://identifiers.org/hco/1/GRCh38#222715912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183075770-C-A

222715912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183075770-C-T

222715919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183075762-G-C

222715923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183075753-T-A

222715923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183075753-T-G

http://identifiers.org/hco/1/GRCh38#222715958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183075718-C-A

222715958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183075718-C-T

222715996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183075680-A-G

222716444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

http://identifiers.org/hco/1/GRCh38#222717965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183074921-C-A

222717965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183074921-C-T

222717974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 183074912-G-T

222718125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183074783-G-A

222718272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183074652-G-T

http://identifiers.org/hco/1/GRCh38#222718338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183074590-A-C

222718582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183074405-T-A

222718845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183074216-A-T

222718877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183074180-T-C

222718877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183074180-T-G

http://identifiers.org/hco/1/GRCh38#222718892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183074169-C-A

222718906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183074155-T-C

222719040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183074028-T-A

222719040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183074028-T-G

222719055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183074013-G-A

222719055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183074013-G-C

222719108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183073965-T-C

222719128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183073945-A-G

222719132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183073875-T-C

222719132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183073875-T-G

222719135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183073872-A-G

222719136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183073871-T-C

http://identifiers.org/hco/1/GRCh38#222719168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183073798-A-C

222719168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183073798-A-T

222719191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183073751-A-G

222719203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183073739-A-G

222719223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183073691-T-G

222719350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183073478-A-G

222719406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183073425-T-C

222719446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183073403-A-G

222719729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183073156-A-G

222720119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183072771-G-C

222720289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183072619-A-G

222720361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183072551-T-G

222720413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183072499-T-A

222722683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183068966-A-G

222722867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183068661-G-A

222722867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183068661-G-C

222722938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183068607-T-C

http://identifiers.org/hco/1/GRCh38#222723052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183068319-A-C

222724044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183067805-A-G

http://identifiers.org/hco/1/GRCh38#222724171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183067681-C-A

222724296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183067308-A-G

222724540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183067096-T-C

222725489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183066665-G-A

222725523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 183066631-A-G

222725572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183066582-A-G

222725572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183066582-A-T

222725581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183066564-T-C

222725603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183066542-A-G

222726235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183066087-T-C

222726933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183066004-C-T

http://identifiers.org/hco/1/GRCh38#222727036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183065919-C-A

222727036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183065919-C-T

222727073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183065876-G-C

222727073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 183065876-G-T

222727618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183065319-C-G

222728106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183064717-C-T

222728132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183064688-G-C

222728132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183064688-G-T

222728823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 183064053-G-A

222728823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 183064053-G-C

222728823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 183064053-G-T

222729214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183063428-G-A

222729274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183063376-G-A

222729274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183063376-G-C

222729334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183063109-A-G

http://identifiers.org/hco/1/GRCh38#222729412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183063028-C-A

http://identifiers.org/hco/1/GRCh38#222729495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183062958-A-C

222729495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183062958-A-G

222729550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183062900-G-T

222729623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 183062855-T-C

222729653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 183062825-A-G

http://identifiers.org/hco/1/GRCh38#222729659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183062819-A-C

222729718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183062754-G-T

http://identifiers.org/hco/1/GRCh38#222729806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183062674-A-C

222729847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183062648-T-G

222729890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183062617-A-G

222729890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183062617-A-T

222729892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183062615-A-G

222729892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183062615-A-T

222730080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: missense variant
orthologous variants: 183062459-G-A

222730206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183062334-A-G

222730683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183062181-A-G

222730742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183062127-C-G

http://identifiers.org/hco/1/GRCh38#222730900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183061587-A-C

222730907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183061580-C-T

222730974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183061524-G-A

222730974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183061524-G-T

222731029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183061483-T-C

222731235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183061307-A-G

http://identifiers.org/hco/1/GRCh38#222731284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183061271-C-A

222731481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, missense_variant
orthologous variants: 183061067-G-A

222731481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, missense_variant
orthologous variants: 183061067-G-T

222731524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 183061024-A-T

222731528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183061020-T-A

222731528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183061020-T-C

222731528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183061020-T-G

222731532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183061016-T-C

http://identifiers.org/hco/1/GRCh38#222731545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183061003-C-A

222731545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183061003-C-G

222731545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183061003-C-T

222731563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183060990-A-G

222731637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183060943-A-G

222731690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183060908-T-C

222731691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183060907-C-T

222731771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183060828-T-A

222732064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183060555-G-A

222732221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron variant
orthologous variants: 183060422-A-T

http://identifiers.org/hco/1/GRCh38#222732582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#183060043-C-A

222732582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: intron_variant, undefined
orthologous variants: 183060043-C-G

222733420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183059597-T-G

222733510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183059515-C-G

222733510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183059515-C-T

http://identifiers.org/hco/1/GRCh38#222733628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183059407-C-A

222733686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183059365-G-A

http://identifiers.org/hco/1/GRCh38#222733865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183059173-C-A

222734010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183059037-T-C

222734222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058839-C-G

222734243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058819-A-G

222734268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058795-A-G

222734320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058748-T-C

222734321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058747-G-T

222734365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058704-T-C

222734386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058683-A-T

222734562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058527-C-G

222734562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058527-C-T

222734828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058273-T-C

222734917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058184-G-T

222734987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058113-A-G

222735002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058097-A-G

222735022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058079-T-C

http://identifiers.org/hco/1/GRCh38#222735043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#183058058-C-A

222735100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183058002-G-T

222735186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26512
most severe consequence: 3 prime UTR variant
orthologous variants: 183057914-A-G