230058492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124948715-C-G

230058640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124948832-T-C

230058674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124948866-A-G

230058674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124948866-A-T

230058691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124948883-G-A

230058722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124948913-C-T

230058746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124948937-C-T

http://identifiers.org/hco/1/GRCh38#230058973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124949123-A-C

230059294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124950759-T-A

230059294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124950759-T-C

http://identifiers.org/hco/1/GRCh38#230059383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124950847-A-C

230059585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124950927-G-A

230059662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124950986-G-A

http://identifiers.org/hco/1/GRCh38#230059709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124951033-A-C

230059757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124951077-C-T

230065645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124956799-A-T

230065724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124956874-G-A

230065736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124956886-G-A

http://identifiers.org/hco/1/GRCh38#230065946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124957071-A-C

230065946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124957071-A-G

230065965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124957090-T-A

230065965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124957090-T-C

230065987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124957105-G-A

230066016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124957134-T-C

230066159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124957336-T-C

http://identifiers.org/hco/1/GRCh38#230066283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124957450-C-A

230066313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124957484-G-T

230066663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124957843-T-C

230066843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124957994-G-T

http://identifiers.org/hco/1/GRCh38#230067120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124958140-C-A

230067120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124958140-C-T

http://identifiers.org/hco/1/GRCh38#230067177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#124958172-C-A

230067177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124958172-C-T

230067328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124958313-G-A

230067328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124958313-G-C

230067328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124958313-G-T

http://identifiers.org/hco/1/GRCh38#230067352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#124958337-C-A

230067352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 124958337-C-G

230067352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 124958337-C-T

230067467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124958426-T-C

230067467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124958426-T-G

http://identifiers.org/hco/1/GRCh38#230067498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124958457-C-A

230067498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124958457-C-G

230067498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124958457-C-T

http://identifiers.org/hco/1/GRCh38#230067509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124958468-A-C

230067509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124958468-A-G

230068016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124958958-C-G

230068033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124958975-G-A

230068525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124959402-G-A

230068848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124959729-G-A

230068868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124959749-A-G

230069006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124959871-G-T

230070151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124961001-C-T

230070441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124961287-T-G

230070645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124961405-T-G

230070867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124961645-C-T

230071400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124962135-G-T

230071410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124962145-G-C

230071524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124962237-T-A

230071720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124962487-G-C

230071767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124962536-A-G

230072389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124963009-T-A

230072448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124963042-C-T

230072516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124963107-C-T

http://identifiers.org/hco/1/GRCh38#230072953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124963643-C-A

230072967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124963661-T-C

230073127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124963825-C-T

230073498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124964190-G-A

230073522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124964214-A-G

http://identifiers.org/hco/1/GRCh38#230073724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124964399-C-A

230076917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124966444-C-G

230077090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124966601-G-T

230077094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124966605-A-G

http://identifiers.org/hco/1/GRCh38#230077326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124966791-A-C

230077636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124966907-T-A

http://identifiers.org/hco/1/GRCh38#230077921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124967173-C-A

230077921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124967173-C-T

230079211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124967924-A-G

230079405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124968082-A-G

http://identifiers.org/hco/1/GRCh38#230079582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124968225-A-C

230079584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124968227-C-T

230079649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124968287-G-A

230079708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124968340-G-A

230080636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124969041-C-G

http://identifiers.org/hco/1/GRCh38#230080680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124969079-C-A

230081020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124969359-T-C

230081324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124969516-C-T

230081350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124969542-T-A

230081399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124969592-T-C

230081595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124969776-C-T

230081596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124969777-A-G

230081813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124969957-G-T

230082111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124970148-G-T

230082232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124970246-G-C

230082384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124970376-G-A

230082387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124970379-G-A

http://identifiers.org/hco/1/GRCh38#230082396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124970388-A-C

230083686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124972231-C-T

230083693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124972238-C-T

230083702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124972240-A-G

230095611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124976463-T-A

230095672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124976525-G-A

230095943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124976769-A-G

230095994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124976818-G-T

230096009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124976833-C-G

230096096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124976938-C-T

http://identifiers.org/hco/1/GRCh38#230096174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124977003-C-A

230096257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124977081-C-T

http://identifiers.org/hco/1/GRCh38#230096553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124977345-A-C

230096573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124977398-T-G

230096589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124977414-A-G

230096589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124977414-A-T

230096611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124977436-A-G

230096632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124977462-C-T

230096698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124977503-T-C

http://identifiers.org/hco/1/GRCh38#230097939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124978394-A-C

230097994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124978459-A-G

230098087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124978613-A-G

230098173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124978695-C-T

230098350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124978833-A-G

230098972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124979019-C-T

230099078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124979101-G-C

230099931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124979335-G-A

230099975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124979377-T-C

230103262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124980803-C-T

230103514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124981089-T-C

230103552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124981126-C-T

http://identifiers.org/hco/1/GRCh38#230103802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124981966-C-A

230103827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124981987-C-T

230103864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124982018-C-G

230103901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124982051-G-A

230104401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124982588-A-G

230104402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124982589-G-C

230104417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124982602-T-C

230105075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124983138-A-G

230105149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124983214-G-A

230105319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124983479-T-C

230105339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124983500-C-T

230105913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124983853-C-G

230105972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124983886-A-G

230106529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124984351-G-C

230110770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124989398-G-T

230111000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124989569-T-C

230111095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124989650-A-G

230111139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124989679-G-A

230111541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124989960-T-A

230111541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124989960-T-C

230111932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124990286-A-T

230111952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124990304-T-C

230111976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124990328-G-A

230112307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124990610-C-T

230112340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124990647-T-G

230112501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124990719-G-A

230112717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124990902-G-C

230113036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124991155-T-A

230113155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124991247-C-G

230113186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124991272-G-T

230113316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124991359-T-C

230113327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124991369-T-C

230113382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124991416-C-T

230113385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124991419-G-A

230113626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124991618-C-T

230113691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124991668-G-A

230113879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124991830-G-T

230114003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124991934-C-T

230114098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124992024-A-T

230114113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124992039-G-A

230120536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124992851-C-G

230120536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124992851-C-T

230120793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124993064-C-T

230122688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124997170-C-T

230122780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124997264-G-C

230122984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124997465-A-T

230123391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124997790-G-A

230123629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124997995-T-G

230123689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124998059-T-C

230123689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124998059-T-G

230123740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124998133-G-A

230123889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124998464-C-G

230124204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124998942-C-G

230124295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999043-C-G

230124399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999095-G-A

230124399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999095-G-C

http://identifiers.org/hco/1/GRCh38#230124484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#124999171-A-C

230124493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999180-A-G

230124570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999238-G-A

230124637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999288-G-A

230124692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999345-T-C

230124744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999391-A-G

230124793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999440-C-T

230124878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999526-T-C

230125107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999738-T-A

230125179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999787-G-A

230125323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999880-A-G

230125405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999955-G-A

230125405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124999955-G-C

http://identifiers.org/hco/1/GRCh38#230125574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125000125-C-A

230125587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125000139-T-A

http://identifiers.org/hco/1/GRCh38#230125694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125000243-C-A

230127711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125001297-G-A

230127723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125001309-C-T

230127756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125001337-C-G

230127756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125001337-C-T

230127757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125001338-G-A

230127899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125001505-A-T

230127923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125001513-A-G

230127923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125001513-A-T

230129047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125002170-G-A

230129047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125002170-G-C

230129120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125002241-C-T

230129188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125002308-T-G

230129200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125002320-A-G

230129233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125002353-C-T

230129251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125002371-T-C

230130446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125003406-G-A

230130521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125003480-C-G

230130614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125003530-C-T

230130640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125003552-C-T

230130806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125003709-A-G

230130837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125003739-G-A

230137851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125004671-T-C

230137968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125004736-C-T

230151248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125009934-C-T

230151257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125009943-A-G

230151272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125009958-C-T

230151293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125009979-C-G

230151316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125010003-A-T

230151361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125010035-C-G

230151361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125010035-C-T

230151373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125010048-G-A

230151463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125010122-G-A

230151585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125010196-G-T

http://identifiers.org/hco/1/GRCh38#230153577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125011076-A-C

230153867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125011368-T-C

230154094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125011545-A-G

230154144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125011594-C-T

230154145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125011595-G-A

230154389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125011904-T-C

230154389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125011904-T-G

230154742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125012242-T-C

230154780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125012278-G-A

230154783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125012281-G-A

230154874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125012350-G-A

230154891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125012367-A-G

230155093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125012499-G-A

230155176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125012523-A-G

230155357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125012657-G-A

230155454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125012748-C-T

230155644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125012959-T-G

230155682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125012976-G-A

230155711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125013003-C-G

230159657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125014364-T-G

230159776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125014480-G-A

http://identifiers.org/hco/1/GRCh38#230159804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125014492-C-A

230160097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125014677-C-T

230161536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125015281-A-T

230161538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125015283-A-G

230165190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125016616-A-G

230169445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125018366-T-A

230169489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125018376-C-T

230169765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125018562-T-A

230169793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125018590-T-A

230171428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125019837-G-A

230171428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125019837-G-C

230176398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125020666-A-G

230176668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125020914-A-G

230176845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125021073-T-C

230176913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125021149-G-A

230176913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125021149-G-T

230177006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125021229-G-A

230177117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125021322-T-A

230177256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125021395-G-A

230177260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125021398-T-A

230177660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125021712-G-A

230177745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125021766-A-G

230177789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125021818-G-A

http://identifiers.org/hco/1/GRCh38#230178184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125022063-C-A

230178188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125022067-T-A

230178199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125022078-A-G

http://identifiers.org/hco/1/GRCh38#230178214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125022093-C-A

230178214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125022093-C-T

230178316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125022195-T-A

230178321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125022207-G-A

http://identifiers.org/hco/1/GRCh38#230178436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125022302-C-A

230178436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125022302-C-G

230178537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125022381-A-G

230192731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125027490-A-G

230192740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125027499-T-C

230192745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125027504-T-C

230193146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125027898-C-G

230194205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125028595-G-A

230194405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125028745-G-A

230194720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125028983-G-C

230194720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125028983-G-T

230202689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125031850-A-G

230202850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125032008-T-C

http://identifiers.org/hco/1/GRCh38#230202990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125032111-C-A

230202990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125032111-C-T

230203033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125032151-G-A

230203104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125032220-C-G

230203104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125032220-C-T

230203174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125032291-T-C

230203473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125032527-T-G

230203607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125032616-A-T

http://identifiers.org/hco/1/GRCh38#230210459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125034882-A-C

230210476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125034901-G-C

230210521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125034960-G-A

230210665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125035092-A-G

230210974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125035395-A-T

230211043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125035446-G-A

230211137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125035502-G-A

230214464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125036169-G-A

230214633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125036329-G-A

230214656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125036352-G-C

230214700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125036392-G-A

230214803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125036474-C-T

230214805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125036476-G-C

230214810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125036481-T-A

230214810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125036481-T-C

230214810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125036481-T-G

230215074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125036692-T-C

230215135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125036747-C-G

230215205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125036802-C-T

230215598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125037101-T-C

230215602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125037105-C-G

230215647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125037140-A-G

230215736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125037229-G-A

230216752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125038151-A-G

230221014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125039418-C-T

230221059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125039492-T-A

230221224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125039612-A-G

http://identifiers.org/hco/1/GRCh38#230221609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125039970-C-A

230221902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125040218-A-G

230222390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125040710-T-G

230222432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125040768-C-T

230222635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125040967-G-T

230224001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125043405-A-G

230224076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125043472-A-G

230224120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125043499-C-T

230224533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125043839-G-A

230224645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125043937-C-G

230224645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125043937-C-T

230224699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125043987-A-G

230225399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125044619-C-T

230225416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125044629-C-G

230232196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048348-A-G

http://identifiers.org/hco/1/GRCh38#230232203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125048355-C-A

230232203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048355-C-T

230232352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048480-G-T

230232360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048487-T-C

230232446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048571-A-G

230232486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048611-C-T

230232617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048727-A-G

230232699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048812-G-A

230232747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048856-C-T

230232871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048940-C-T

230232919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125048970-A-G

230232976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049041-G-A

230232976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049041-G-T

230233076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049159-T-C

230233082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049165-T-C

230233223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049281-T-C

230234807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049652-G-A

230234807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125049652-G-T

230235641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125050069-G-A

http://identifiers.org/hco/1/GRCh38#230235659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125050087-A-C

230235969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125050364-G-A

230236089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125050486-G-A

230236089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125050486-G-C

230236089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125050486-G-T

230236126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125050523-A-G

http://identifiers.org/hco/1/GRCh38#230236335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125050713-C-A

230236335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125050713-C-G

230236497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125050835-T-C

230236531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125050884-A-T

http://identifiers.org/hco/1/GRCh38#230236557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125050908-C-A

230236557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125050908-C-T

230236613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125050963-T-A

230236613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125050963-T-C

230236858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125052219-G-A

230236858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125052219-G-T

230237119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125052478-T-A

230242006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125053889-T-C

230242177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054026-T-C

230242209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054058-G-A

230242209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054058-G-C

230242209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054058-G-T

230243096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054674-A-G

230243140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054711-C-G

230243140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054711-C-T

http://identifiers.org/hco/1/GRCh38#230243165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125054730-C-A

230243165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054730-C-T

http://identifiers.org/hco/1/GRCh38#230243180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125054742-C-A

230243180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054742-C-T

230243221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054767-G-A

230243221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054767-G-T

http://identifiers.org/hco/1/GRCh38#230243261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125054784-C-A

230243275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054802-T-A

230243275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054802-T-G

http://identifiers.org/hco/1/GRCh38#230243276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125054803-C-A

230243276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054803-C-G

230243296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054821-G-A

230243296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125054821-G-T

230243302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125054827-G-A

230243302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125054827-G-T

http://identifiers.org/hco/1/GRCh38#230243334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125054859-C-A

230243334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125054859-C-T

http://identifiers.org/hco/1/GRCh38#230243562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125054998-C-A

230243562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125054998-C-T

230243576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125055012-A-G

230243987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125055258-G-A

http://identifiers.org/hco/1/GRCh38#230244117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125055382-A-C

230244198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125055454-T-C

230244326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125055529-G-C

230244965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125055904-G-C

230245019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125055960-G-C

230246174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125056567-T-A

http://identifiers.org/hco/1/GRCh38#230246176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125056568-C-A

http://identifiers.org/hco/1/GRCh38#230246245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125056621-C-A

230246245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125056621-C-T

230246249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125056625-G-A

230249035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058585-C-G

230249035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058585-C-T

230249064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058622-G-A

230249064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058622-G-T

230249107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058666-A-T

230249115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058674-A-G

230249132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058690-G-T

230249283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058844-C-T

230249284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058845-A-G

http://identifiers.org/hco/1/GRCh38#230249344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125058902-A-C

230249388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058939-G-A

230249388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058939-G-C

230249388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058939-G-T

230249415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058963-A-G

230249415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058963-A-T

230249435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125058983-A-G

230250327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125059212-G-C

230250327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125059212-G-T

230250484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: missense variant
orthologous variants: 125059334-T-G

http://identifiers.org/hco/1/GRCh38#230250659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125059502-C-A

http://identifiers.org/hco/1/GRCh38#230250681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125059511-C-A

http://identifiers.org/hco/1/GRCh38#230250700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125059522-C-A

230250788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125059580-G-A

230250940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125059726-A-G

230250968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125059754-G-A

230251129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125059882-A-G

230251222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125059945-A-G

230251523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125060259-G-A

230251607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125060316-A-G

230251636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron variant
orthologous variants: 125060344-A-G

230255246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: synonymous variant
orthologous variants: 125061042-T-C

230255431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125061212-G-T

http://identifiers.org/hco/1/GRCh38#230261137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125062453-A-C

230261137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125062453-A-T

230261170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125062481-G-A

230261186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125062496-A-G

http://identifiers.org/hco/1/GRCh38#230261275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125062573-C-A

230261294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125062592-A-G

230262484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125063195-C-T

http://identifiers.org/hco/1/GRCh38#230262505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125063244-C-A

230262506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125063245-A-G

230262627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 125063367-T-C

http://identifiers.org/hco/1/GRCh38#230263070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125064144-C-A

230263105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125064172-G-A

230263105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125064172-G-C

http://identifiers.org/hco/1/GRCh38#230263144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125064210-C-A

230265118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125065078-C-G

230265221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125065157-A-T

230265349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 125065290-C-T

230265371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125065312-T-C

230265385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125065321-C-T

230265408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125065344-A-T

230270554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125065910-G-A

230270708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125066027-G-A

230270728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125066047-T-G

230274407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125067523-T-C

230274417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125067533-G-A

230274430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125067546-G-A

230274568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125067681-C-T

230276367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125068380-C-T

230276423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125068432-G-A

230276576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125068582-C-T

230276582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125068588-G-C

230276804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125068770-C-T

230276929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125068789-T-C

230277059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125068879-G-T

230277491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125069178-A-G

230277517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125069206-G-A

230277541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125069222-G-A

230277681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125069343-C-T

230277743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125069382-G-A

http://identifiers.org/hco/1/GRCh38#230277928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125069552-A-C

230278038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125069658-G-A

230278079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125069700-G-A

230278079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125069700-G-T

230279413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125070152-G-A

230279413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125070152-G-C

230279579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070305-G-C

230279579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070305-G-T

230279599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070335-G-A

230279599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070335-G-T

http://identifiers.org/hco/1/GRCh38#230279611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125070347-C-A

230279611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070347-C-G

230279611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070347-C-T

http://identifiers.org/hco/1/GRCh38#230279725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125070437-C-A

230279725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070437-C-G

http://identifiers.org/hco/1/GRCh38#230279734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125070446-C-A

230279734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070446-C-T

http://identifiers.org/hco/1/GRCh38#230279752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125070452-A-C

230279752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070452-A-G

http://identifiers.org/hco/1/GRCh38#230279809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125070503-C-A

230279856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070539-G-A

230279856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070539-G-C

230279865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070548-T-C

230279943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070647-G-A

230280127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070867-A-G

http://identifiers.org/hco/1/GRCh38#230280233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125070920-C-A

230280239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070926-G-A

230280239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070926-G-T

230280244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070931-T-G

230280264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070945-G-A

230280264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070945-G-T

230280267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070948-G-A

230280292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070972-G-A

230280307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070988-G-T

230280318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125070999-G-A

230280405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125071085-T-C

http://identifiers.org/hco/1/GRCh38#230280429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125071112-A-C

230280571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125071250-G-A

230280571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125071250-G-C

230280630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125071312-G-A

230280630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125071312-G-T

http://identifiers.org/hco/1/GRCh38#230280650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125071328-C-A

230280650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125071328-C-T

230280701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125071361-C-G

230280701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125071361-C-T

230280777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125071395-G-A

230280777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125071395-G-T

230280805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125071420-A-G

http://identifiers.org/hco/1/GRCh38#230280853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125071446-C-A

230280936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 125071502-C-T

230280948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125071514-T-C

230281038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125071531-T-C

230281038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125071531-T-G

230281043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125071536-G-T

230281236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125071680-G-A

230281236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125071680-G-T

230281385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125071821-C-T

230281458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125071882-A-G

http://identifiers.org/hco/1/GRCh38#230281490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125071912-C-A

230281491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 125071913-T-C

230281501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125071923-T-C

230281536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125071963-C-T

230281718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125072060-A-G

http://identifiers.org/hco/1/GRCh38#230281733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125072075-C-A

230281733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125072075-C-G

230281733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125072075-C-T

230281746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125072088-T-C

230281746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125072088-T-G

http://identifiers.org/hco/1/GRCh38#230281813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4124
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#125072151-A-C