http://identifiers.org/hco/11/GRCh38#113409685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49319397-C-A

http://identifiers.org/hco/11/GRCh38#113409686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49319396-C-A

113409686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49319396-C-T

113409808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49319278-G-T

113409809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49319277-A-G

113409810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49319276-G-A

113409958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49319178-A-G

http://identifiers.org/hco/11/GRCh38#113410000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49319135-A-C

http://identifiers.org/hco/11/GRCh38#113410040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49319083-C-A

113410040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49319083-C-T

http://identifiers.org/hco/11/GRCh38#113410056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49319066-A-C

113410072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49319050-T-C

http://identifiers.org/hco/11/GRCh38#113410076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49319046-C-A

113410076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49319046-C-T

113410122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318995-G-A

113410122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318995-G-T

113410146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318971-G-A

113410146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318971-G-T

http://identifiers.org/hco/11/GRCh38#113410206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49318912-A-C

113410222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318896-T-G

113410239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318879-G-A

113410362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318748-G-T

113410370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318740-G-A

113410370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318740-G-T

http://identifiers.org/hco/11/GRCh38#113410371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49318739-C-A

113410371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318739-C-T

113410403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318713-C-T

113410491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318627-G-A

113410491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318627-G-T

113410501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318618-G-A

113410501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318618-G-C

113410501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49318618-G-T

113410946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318174-G-A

113410946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318174-G-C

113410946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318174-G-T

113411006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318099-A-G

113411006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318099-A-T

http://identifiers.org/hco/11/GRCh38#113411029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49318064-C-A

113411044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318049-G-A

113411044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318049-G-T

http://identifiers.org/hco/11/GRCh38#113411414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49317621-C-A

113411414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49317621-C-T

113411415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49317620-G-A

113411415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49317620-G-T

http://identifiers.org/hco/11/GRCh38#113411490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49317544-C-A

113411490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49317544-C-T

http://identifiers.org/hco/11/GRCh38#113411583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49317501-A-C

113411583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49317501-A-G

113411583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49317501-A-T

http://identifiers.org/hco/11/GRCh38#113411600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49317494-C-A

113411600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49317494-C-T

113411625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49317477-G-A

113411648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49317454-G-A

113411648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49317454-G-T

113411691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49317421-G-A

113411691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49317421-G-T

113411775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49317336-A-G

113411775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49317336-A-T

http://identifiers.org/hco/11/GRCh38#113411786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49317325-C-A

113411786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49317325-C-T

http://identifiers.org/hco/11/GRCh38#113411914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49317203-C-A

113412230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49316681-A-G

113412230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49316681-A-T

http://identifiers.org/hco/11/GRCh38#113412284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49316638-C-A

http://identifiers.org/hco/11/GRCh38#113412312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49316613-C-A

113412373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49316573-C-T

113412433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49316518-G-T

113412690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: missense variant
orthologous variants: 49316246-G-T

113412705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: missense variant
orthologous variants: 49316228-T-C

113412789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: missense variant
orthologous variants: 49316144-T-G

113412901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49316032-G-A

113412901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49316032-G-C

113412901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49316032-G-T

113412964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49315981-T-C

113413111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49315829-T-A

113413296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49315643-T-C

113413380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49315593-T-A

113413385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49315588-T-G

113413769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49315214-A-G

http://identifiers.org/hco/11/GRCh38#113413784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49315200-C-A

113413822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49315162-T-G

http://identifiers.org/hco/11/GRCh38#113413823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49315161-A-C

113413823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron variant
orthologous variants: 49315161-A-G

113413888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49315073-T-A

113413888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49315073-T-G

113413899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49315062-G-A

113413899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49315062-G-T

113413912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49315049-G-T

113413932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49315029-T-C

113413936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49315025-G-C

113413936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49315025-G-T

113413953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49315008-G-A

http://identifiers.org/hco/11/GRCh38#113414031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49314918-C-A

113414031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49314918-C-T

http://identifiers.org/hco/11/GRCh38#113414063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49314895-C-A

113414063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49314895-C-T

http://identifiers.org/hco/11/GRCh38#113414255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49314701-A-C

113414271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49314684-G-T

113414309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49314649-C-T

113414531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49314415-C-T

113414596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49314348-G-A

113414596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49314348-G-T

113414600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49314344-G-A

113414600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49314344-G-C

113414600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49314344-G-T

http://identifiers.org/hco/11/GRCh38#113414608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49314337-A-C

http://identifiers.org/hco/11/GRCh38#113414931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49314017-C-A

113415087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313882-G-A

http://identifiers.org/hco/11/GRCh38#113415181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49313767-A-C

113415181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313767-A-G

113415181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313767-A-T

http://identifiers.org/hco/11/GRCh38#113415185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49313763-A-C

113415185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313763-A-G

113415185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313763-A-T

http://identifiers.org/hco/11/GRCh38#113415186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49313762-A-C

113415186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313762-A-G

113415186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313762-A-T

113415264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313690-G-A

113415264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313690-G-T

113415337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49313630-A-G

113415341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49313627-C-T

113415354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49313614-T-A

113415536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49313438-A-G

113415639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313333-G-A

113415649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313323-G-A

113415649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313323-G-C

113415751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313233-T-A

113415751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313233-T-C

113415792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313186-G-A

113416429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49312576-C-T

113416630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49312394-T-A

113416630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49312394-T-C

113416661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49312360-C-T

113416822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49312215-C-T

113416972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 49312069-C-T

http://identifiers.org/hco/11/GRCh38#113417024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49312018-C-A

113417025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49312017-T-A

113417025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49312017-T-C

113417115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311950-A-G

http://identifiers.org/hco/11/GRCh38#113417142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49311934-A-C

113417142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311934-A-G

113417154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311922-G-A

113417193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311910-A-G

113417204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311899-C-T

http://identifiers.org/hco/11/GRCh38#113417251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49311856-C-A

113417251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311856-C-T

113417286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311828-A-G

113417295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311824-A-T

113417354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311770-G-A

113417394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311731-T-C

113417522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311568-G-A

http://identifiers.org/hco/11/GRCh38#113417702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49311417-C-A

113417751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311368-T-G

113417756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311363-C-G

113417825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311308-G-A

113417850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311299-G-A

113417850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311299-G-T

113417857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311292-T-C

http://identifiers.org/hco/11/GRCh38#113417897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49311252-C-A

http://identifiers.org/hco/11/GRCh38#113417898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49311251-A-C

113417946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311221-C-G

113417946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311221-C-T

113417948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311219-C-T

113417992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311178-G-A

113417992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311178-G-C

113417992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311178-G-T

113417993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311177-C-T

113418053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49311117-C-T

113418154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311016-T-A

http://identifiers.org/hco/11/GRCh38#113418156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49311014-A-C

113418156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311014-A-G

113418156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311014-A-T

113418334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49310451-C-T

113418347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49310438-A-T

http://identifiers.org/hco/11/GRCh38#113418433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49310344-C-A

113418506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49310271-T-C

113418557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49310225-G-A

113418557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49310225-G-C

113419690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49310102-C-T

113420012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309863-G-A

113420106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309773-T-G

113422106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309066-G-A

113422129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309043-A-T

113422438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308816-C-T

113422476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308777-C-T

113423673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307858-A-G

113423890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307651-T-G

113423924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307617-T-A

113423924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307617-T-C

113424031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307505-C-T

113424122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307411-C-T

113424237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307300-G-A

113424237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307300-G-C

113424237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307300-G-T

113424243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307294-G-C

113424243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307294-G-T

http://identifiers.org/hco/11/GRCh38#113424260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49307277-A-C

113424260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307277-A-G

http://identifiers.org/hco/11/GRCh38#113424265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49307272-C-A

http://identifiers.org/hco/11/GRCh38#113424304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49307248-C-A

113424304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307248-C-T

113424699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49306866-G-C

113424701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49306864-C-T

113424717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49306848-G-A

113424718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49306847-A-G

http://identifiers.org/hco/11/GRCh38#113424781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49306771-C-A

113424781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49306771-C-T

113424830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49306723-G-A

113424830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49306723-G-C

http://identifiers.org/hco/11/GRCh38#113424978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49306606-A-C

http://identifiers.org/hco/11/GRCh38#113424979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49306605-C-A

113424979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49306605-C-G

113425029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49306565-G-A

113425029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49306565-G-C

113425029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49306565-G-T

113425082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49306513-T-C

113425302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49306038-G-A

113425404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305976-G-T

113425431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305948-T-C

113425469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305912-G-T

113425557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305846-C-G

113425557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305846-C-T

113425928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305553-A-G

113426077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305161-T-G

113426084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305154-A-T

113426429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49304834-A-T

http://identifiers.org/hco/11/GRCh38#113426695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49304690-C-A

113426697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49304688-A-G

113426952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49304458-G-T

113427192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49304161-C-T

113427382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49303723-C-T

113427521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49303610-C-T

113427533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49303598-A-G

http://identifiers.org/hco/11/GRCh38#113427553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49303578-A-C

113427557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49303574-C-T

113427662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49303467-C-T

http://identifiers.org/hco/11/GRCh38#113427673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49303456-A-C

113427673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49303456-A-G

http://identifiers.org/hco/11/GRCh38#113427891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49303247-C-A

113427931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49303205-T-G

113430188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49303114-A-G

113430271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49303044-C-T

113430305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49303010-C-T

113430404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302950-T-C

113430508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302853-G-A

113430627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302752-T-C

113430642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302737-G-A

113430753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302622-C-T

113430787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302585-G-A

113430859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302513-C-T

113431109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302305-A-G

113431140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302273-A-G

113431288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302128-C-T

http://identifiers.org/hco/11/GRCh38#113431307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49302102-C-A

113431433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301993-G-A

113431469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301958-A-G

113431495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301926-A-G

113431671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301745-A-G

113431775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301660-G-A

113431992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301467-G-A

113432097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301338-G-A

113432286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301211-C-G

113432286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301211-C-T

113432327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301189-C-T

113432381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49301157-A-G

113432620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300908-G-A

113432636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300896-C-T

113432932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300648-G-A

113433082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49300443-G-C

113433430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49299773-A-G

113433480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49299734-G-A

113433509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49299704-G-A

113433527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49299686-C-T

113434253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49298758-G-A

113434253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49298758-G-C

113434418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49298581-C-T

113434538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49298475-G-A

113434550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49298466-C-T

113434639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49298404-A-G

113434726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49298320-C-T

113434786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49298267-A-G

http://identifiers.org/hco/11/GRCh38#113434804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49298250-C-A

113434811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49298243-G-A

113434967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49298119-G-A

113434987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49298064-C-T

113435017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49298036-C-T

113435039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49298012-T-C

113435173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49297874-C-T

113435632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49297359-C-T

http://identifiers.org/hco/11/GRCh38#113435878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49297071-C-A

113436069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296840-C-T

113436122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296791-T-C

113436158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296753-A-G

113436318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296621-A-G

113436320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296619-G-A

113436320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296619-G-T

113436322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296617-A-G

113436348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296562-G-A

113436353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296557-T-C

113436385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296525-C-T

113436490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296424-A-G

113436538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296198-G-A

113436538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296198-G-T

113436663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296038-C-T

113436664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296037-G-A

113436677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49295853-G-A

113436793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49295740-G-A

113436889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49295653-G-A

113437185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49295365-G-A

113437191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49295359-C-G

113437197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49295353-T-C

113437501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49294816-G-C

113437850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49294417-G-T

113437956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49294313-G-C

113437956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49294313-G-T

113437957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49294312-G-A

113438298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49293945-T-A

http://identifiers.org/hco/11/GRCh38#113438473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49293766-A-C

113438480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49293759-A-G

http://identifiers.org/hco/11/GRCh38#113438528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49293712-C-A

http://identifiers.org/hco/11/GRCh38#113438615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49293632-A-C

113438660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49293591-G-A

113438837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49293418-C-G

113439041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49293207-G-A

113440846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49292317-A-G

113440968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49292199-A-T

113441076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49292093-A-G

113441092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49292071-G-A

113441331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49291846-C-T

113441458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49291734-A-G

113441478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49291720-A-G

113442339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49291052-C-T

113442342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49291049-G-A

113442346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49291045-T-C

http://identifiers.org/hco/11/GRCh38#113442522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49290900-A-C

113442581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49290858-C-T

http://identifiers.org/hco/11/GRCh38#113442594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49290847-A-C

http://identifiers.org/hco/11/GRCh38#113442719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49290681-C-A

113442821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49290583-G-A

113442889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49290517-C-T

113442910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49290505-A-G

113443149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49290288-A-G

113443149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49290288-A-T

113443246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49290213-A-T

113443285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49290170-A-G

113443377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49290085-T-C

113443522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49289946-G-A

113443550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49289907-C-T

113443575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49289859-A-G

113443749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49289479-T-C

113443854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49289318-G-A

http://identifiers.org/hco/11/GRCh38#113444904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49286222-C-A

http://identifiers.org/hco/11/GRCh38#113445100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49286022-C-A

113445100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49286022-C-T

113445161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49285959-T-C

113446475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49285095-C-T

113446645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49284928-G-A

113446654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49284919-G-C

http://identifiers.org/hco/11/GRCh38#113447460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49283118-C-A

113447527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49283077-G-A

113447624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49282984-G-T

113447628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49282980-G-C

113447647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49282961-G-A

113447660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49282948-G-T

http://identifiers.org/hco/11/GRCh38#113447661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49282947-A-C

113447661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49282947-A-G

113447687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49282921-A-G

113447719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49282890-G-T

113447738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49282872-G-T

http://identifiers.org/hco/11/GRCh38#113447751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49282860-A-C

http://identifiers.org/hco/11/GRCh38#113447768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49282843-C-A

113447787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49282824-G-A

113447787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49282824-G-T

113447989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49282644-T-A

113447989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49282644-T-C

113448147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49282502-G-C

113448324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49282321-G-A

113448624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49282064-G-A

113448964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49281831-G-A

113449032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49281786-T-C

113449137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49281718-T-G

113449372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49281510-G-A

113449431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49281445-G-A

113449598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49281292-T-C

113450079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49280782-G-A

113450393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49280455-C-G

113450505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49280344-C-T

113450870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49280024-C-T

113450994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49279911-G-A

113451074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49279835-C-T

113451117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49279792-G-A

113451117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49279792-G-C

113451153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49279755-G-A

113451153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49279755-G-C

113451164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49279744-A-G

113451299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49279643-G-T

113451322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49279621-G-A

113451322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49279621-G-C

113451425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49279526-C-G

113451579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49279203-C-G

113451600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49279176-C-T

113451694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49279091-C-T

113451974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49278769-T-C

113451993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49278750-C-T

113452299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49278563-A-G

113452436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49278370-G-A

113452442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49278364-G-A

113452442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49278364-G-C

113452448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49278358-G-A

113452449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49278357-T-A

113452449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49278357-T-C

113452474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49278332-G-A

113452474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49278332-G-T

113452506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49278300-T-C

113452506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49278300-T-G

113452514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49278292-T-G

113453292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49277810-G-A

113453364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49277732-T-C

113453388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49277708-G-C

113453401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49277695-T-C

113453593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49277538-T-G

113453653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49277479-G-T

113453715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49277425-C-T

113453804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49277340-T-A

113454210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49276971-G-A

113456166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49274897-T-C

113456471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49274590-C-T

http://identifiers.org/hco/11/GRCh38#113456562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49274364-C-A

113456562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49274364-C-T

113456971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49273739-C-T

113457020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49273675-G-A

113457175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49273393-G-A

113457221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49273344-A-G

113457276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49273294-G-T

113457293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49273276-C-G

113457310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49273259-C-G

113457310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49273259-C-T

http://identifiers.org/hco/11/GRCh38#113457984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49271939-C-A

113457984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49271939-C-T

113458004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49271919-C-T

113458036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49271882-G-A

113458573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49271378-G-T

113458591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49271360-C-T

113458963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49271104-G-A

113458984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49271083-A-G

113459116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49270965-C-T

113460119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49269813-A-G

113460187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49269747-C-T

http://identifiers.org/hco/11/GRCh38#113460408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49269422-C-A

113460408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49269422-C-G

113460419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49269411-G-A

http://identifiers.org/hco/11/GRCh38#113460459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49269359-A-C

http://identifiers.org/hco/11/GRCh38#113460604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49269253-C-A

113460682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49269172-C-G

113460899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49268953-T-C

113461283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49268715-G-A

113461365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49268653-C-T

113461820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49268219-C-T

113461862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49268205-G-T

113461927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49268191-C-G

113461927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49268191-C-T

113462387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49267766-T-A

113462387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49267766-T-C

113462399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49267754-G-A

113462501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49267666-G-C

113462624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49267531-T-C

113462624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49267531-T-G

113462703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49267362-G-A

113462868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49267141-G-A

113463216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49266602-A-T

http://identifiers.org/hco/11/GRCh38#113463312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49266560-A-C

113463328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49266544-A-G

113463378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49266492-C-T

113463397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49266473-A-G

113463410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49266454-G-T

113463414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49266450-G-A

113463480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49266382-G-T

113463617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49266228-C-T

113463876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49265969-G-A

113463877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49265968-G-A

113463946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49265899-T-C

113463984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49265819-A-G

113464174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49265644-G-A

113464182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49265627-G-C

http://identifiers.org/hco/11/GRCh38#113464186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49265623-C-A

113464679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49265195-C-G

113464855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49265004-C-T

113464884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49264974-A-G

113464987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49264900-C-G

http://identifiers.org/hco/11/GRCh38#113465873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49263876-C-A

113466911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49260232-G-T

113466949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49260202-T-G

113467017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49260144-G-A

113467166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49260038-G-A

http://identifiers.org/hco/11/GRCh38#113467474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49259750-C-A

113467581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49259359-C-T

http://identifiers.org/hco/11/GRCh38#113467658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49259264-A-C

http://identifiers.org/hco/11/GRCh38#113467748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49259175-A-C

113467776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49259147-G-A

113467956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49258975-T-C

113468251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49258695-C-G

113469050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49258157-A-G

113469243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49257999-C-G

113470035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49256738-G-A

113470035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49256738-G-C

113470270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49256495-G-A

113470340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49256424-G-A

113470941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49255860-A-G

113471088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49255718-A-G

113471089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49255717-C-T

113471130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49255678-C-T

http://identifiers.org/hco/11/GRCh38#113471140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49255668-C-A

113471143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49255665-T-G

113471202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49255619-A-G

113471352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49255475-C-T

113471485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49255326-A-G

113471494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49255317-T-A

http://identifiers.org/hco/11/GRCh38#113471519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49255288-C-A

113472020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49254844-A-G

http://identifiers.org/hco/11/GRCh38#113472033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49254831-C-A

113472102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49254764-T-C

113472268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49254611-G-C

113472479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49254397-T-A

113472479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49254397-T-C

http://identifiers.org/hco/11/GRCh38#113472573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49254327-C-A

113472732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49254168-G-A

113472909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49254010-A-T

113473188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49253781-A-G

http://identifiers.org/hco/11/GRCh38#113473354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49253717-C-A

113473354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49253717-C-T

113473889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49253088-G-T

http://identifiers.org/hco/11/GRCh38#113474039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49252943-A-C

113474196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49252801-A-G

113474227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49252770-T-A

113474227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49252770-T-C

http://identifiers.org/hco/11/GRCh38#113474399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#49252607-C-A

113474399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49252607-C-T

113474424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49252582-T-C

http://identifiers.org/hco/11/GRCh38#113474531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#49252482-C-A

113474531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49252482-C-T

http://identifiers.org/hco/11/GRCh38#113474561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#49252452-C-A

113474617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49252400-G-A

113474655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49252363-G-A

113475025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49252072-C-G

http://identifiers.org/hco/11/GRCh38#113475062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49252036-C-A

113475062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49252036-C-T

113475132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49251966-G-A

113475132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49251966-G-T

113475154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49251944-G-A

113475154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49251944-G-C

113475350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49251758-A-G

http://identifiers.org/hco/11/GRCh38#113475493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49251588-A-C

113475504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49251577-T-A

113475504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49251577-T-C

113475630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49251440-A-G

http://identifiers.org/hco/11/GRCh38#113475633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#49251437-C-A

113475667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: non coding transcript exon variant
orthologous variants: 49251392-G-A

113475667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3023
most severe consequence: non coding transcript exon variant
orthologous variants: 49251392-G-T