http://identifiers.org/hco/12/GRCh38#13196741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135339967-C-A

13196765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135339991-G-A

13196765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135339991-G-T

13196880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135340108-A-G

13196976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135340190-T-C

13197116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135340282-G-A

13197238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135340407-A-G

13197333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135340579-A-G

13198352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135341254-C-T

13198431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135341350-G-A

13198616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135341542-G-A

13198822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135341780-T-A

13198891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135341835-G-C

http://identifiers.org/hco/12/GRCh38#13198973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135341928-A-C

13198986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135341939-G-C

13199145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135342108-A-G

13199176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135342139-A-G

13199176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135342139-A-T

http://identifiers.org/hco/12/GRCh38#13199192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135342154-C-A

13199192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135342154-C-T

13199196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135342157-T-C

13199308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135342262-T-A

13199308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135342262-T-C

13199322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135342276-A-T

13199379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135342328-G-T

13199402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135342332-A-G

13199414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135342340-G-A

13199658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135342743-G-A

13199689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135342780-C-T

13199934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135343097-G-A

13199946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135343113-C-G

13199952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135343119-C-T

13199970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135343327-T-C

13200138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135343535-T-A

13200138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135343535-T-G

13200545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135343763-T-C

13200592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135343807-C-T

http://identifiers.org/hco/12/GRCh38#13200657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135343869-C-A

13200777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135343992-G-A

13200848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135344069-T-C

13201013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135344207-A-G

http://identifiers.org/hco/12/GRCh38#13201639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135344510-C-A

13201639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135344510-C-T

13201977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135344795-G-A

13201985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135344803-A-T

13202007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135344825-G-A

http://identifiers.org/hco/12/GRCh38#13202057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135344853-C-A

13202058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135344854-A-G

http://identifiers.org/hco/12/GRCh38#13202245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135345033-A-C

13202281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135345056-G-C

13202352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135345107-G-A

13202368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135345116-G-A

13202410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135345157-G-C

13202613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135345359-G-T

http://identifiers.org/hco/12/GRCh38#13202757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135345493-A-C

13202782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135345512-G-A

13203337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135346828-G-A

13203399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135346888-G-T

http://identifiers.org/hco/12/GRCh38#13203508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135347014-A-C

13203609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135347108-T-C

http://identifiers.org/hco/12/GRCh38#13204005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135347614-C-A

13204169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135347808-C-G

13204382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135348015-C-T

13204430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135348062-G-C

13204589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135348224-T-A

13204644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135348281-G-A

13205478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135349211-T-C

13205492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135349219-G-A

13205492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135349219-G-C

13205820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135349532-T-A

13205823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135349535-A-T

13205856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135349566-G-A

13205910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135349613-G-A

http://identifiers.org/hco/12/GRCh38#13205916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135349619-A-C

13206294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135349995-A-G

13207604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135350187-T-C

13207691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135350266-C-T

13207703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135350278-G-T

13207840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135350406-T-C

13207986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135350555-T-C

13208509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135351309-G-A

13208713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135351497-G-C

13208840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135351659-T-C

13208891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135351713-G-A

13208891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135351713-G-T

13208988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135351800-A-G

13209153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135351946-G-T

http://identifiers.org/hco/12/GRCh38#13209159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135351952-C-A

13209159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135351952-C-G

13209187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135351978-A-G

13209345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135352079-G-A

13209345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135352079-G-T

13209368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135352102-T-C

http://identifiers.org/hco/12/GRCh38#13209426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135352162-C-A

13209433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135352169-T-C

13209434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135352170-C-T

13209601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135352329-G-C

13209601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135352329-G-T

13209622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135352375-A-G

http://identifiers.org/hco/12/GRCh38#13209693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135352445-A-C

http://identifiers.org/hco/12/GRCh38#13209811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135352577-A-C

13209920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135352669-G-A

13209920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135352669-G-T

13209984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135352739-G-C

13210299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135353016-C-T

13210346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135353072-A-G

13210346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135353072-A-T

13210376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135353097-C-G

13210438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135353138-T-C

13210531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135353225-A-G

13210673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135353364-A-G

13210771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135353459-A-G

13210831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135353519-C-G

13210860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135353548-T-C

13210873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135353560-C-G

13210873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135353560-C-T

13210880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135353567-G-A

13211135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135353822-A-G

13211435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135354141-G-A

13211479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135354184-G-C

13211479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135354184-G-T

13211855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135354565-T-C

13211876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135354580-G-A

13211876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135354580-G-T

13211879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135354583-G-A

13211879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135354583-G-T

13211883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135354587-G-A

13211883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135354587-G-T

13211890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135354594-A-G

13211895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135354599-G-A

13211895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135354599-G-T

http://identifiers.org/hco/12/GRCh38#13211911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135354607-C-A

13211911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135354607-C-T

13211929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135354619-A-G

13211987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135354673-G-A

13211987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135354673-G-T

http://identifiers.org/hco/12/GRCh38#13211988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135354674-C-A

13211988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135354674-C-T

13212012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135354698-G-T

http://identifiers.org/hco/12/GRCh38#13212015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135354701-A-C

13212015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135354701-A-T

13212291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135354962-A-G

13212356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135355019-C-T

13212478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135355602-A-G

13212495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135355620-A-G

http://identifiers.org/hco/12/GRCh38#13212564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135355692-A-C

13212707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135355814-G-A

13212707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135355814-G-T

http://identifiers.org/hco/12/GRCh38#13212718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135355825-A-C

13212718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135355825-A-G

13212755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135355848-G-A

13212795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135355880-A-G

13212859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135355932-A-G

13212994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135356069-C-T

13213125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135356577-T-C

http://identifiers.org/hco/12/GRCh38#13213181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135356634-A-C

13213193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135356646-T-G

13213354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135356784-G-A

13213376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135356806-A-T

http://identifiers.org/hco/12/GRCh38#13213404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135356834-C-A

13213404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135356834-C-T

13213440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135356865-C-G

13213440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135356865-C-T

13213443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135356868-G-T

http://identifiers.org/hco/12/GRCh38#13213694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135357112-A-C

13213694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135357112-A-G

13213742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135357160-C-T

13213799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135357217-A-G

13213799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135357217-A-T

13213847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135357266-G-A

13213847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135357266-G-C

http://identifiers.org/hco/12/GRCh38#13214093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135357550-A-C

13214180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135357633-C-G

13214180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135357633-C-T

http://identifiers.org/hco/12/GRCh38#13214232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135357679-C-A

13214258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135357706-A-T

13214264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135357712-G-T

http://identifiers.org/hco/12/GRCh38#13214304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135357752-C-A

13214304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135357752-C-T

http://identifiers.org/hco/12/GRCh38#13214477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135357920-C-A

13214477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135357920-C-T

13214658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135358105-C-T

http://identifiers.org/hco/12/GRCh38#13214712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135358158-A-C

13214814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135358272-G-A

13214814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135358272-G-C

13214814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135358272-G-T

13214885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135358350-G-A

13214893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135358358-G-T

13214898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135358363-T-C

13214982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135358442-T-G

13215018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135358491-T-C

13215018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135358491-T-G

http://identifiers.org/hco/12/GRCh38#13215052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135358526-C-A

13215052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135358526-C-T

http://identifiers.org/hco/12/GRCh38#13215079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135358553-C-A

13215079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135358553-C-G

http://identifiers.org/hco/12/GRCh38#13215152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135358622-C-A

13215152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135358622-C-T

13215266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135358718-G-A

13215266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135358718-G-T

http://identifiers.org/hco/12/GRCh38#13215290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135358742-C-A

13215290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135358742-C-T

13215379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135358842-T-C

13215410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135358873-T-G

13215483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135358939-G-A

13215483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135358939-G-T

13215495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135358951-A-G

13215504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135358960-A-G

13215571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359027-G-T

13215634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359088-T-C

13215707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359159-G-A

13215714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359166-G-A

13215723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359175-G-T

http://identifiers.org/hco/12/GRCh38#13215766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135359218-C-A

13215766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359218-C-T

13215849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359305-G-C

13215889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359345-G-A

13215889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359345-G-T

13215894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359350-T-C

13215905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359361-A-G

http://identifiers.org/hco/12/GRCh38#13215927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135359381-C-A

13215927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359381-C-T

http://identifiers.org/hco/12/GRCh38#13215946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135359396-C-A

13215946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359396-C-T

13215973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359427-G-A

13215973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359427-G-T

http://identifiers.org/hco/12/GRCh38#13215986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135359442-C-A

13216058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359509-G-A

13216058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359509-G-T

13216225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359630-C-G

13216225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359630-C-T

13216422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135359827-G-C

http://identifiers.org/hco/12/GRCh38#13216520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135359918-C-A

13216520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135359918-C-T

13216583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135359982-A-G

13216604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135360003-T-C

http://identifiers.org/hco/12/GRCh38#13216675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135360074-C-A

13216675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135360074-C-T

13216776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135360175-T-C

13216887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135360288-G-T

13217991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135362799-T-C

13218064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135362870-G-A

13218305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363108-T-G

13218587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363367-G-C

13218597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363377-G-T

13218644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363403-G-A

13218644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363403-G-T

13218663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363416-G-A

13218663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363416-G-T

http://identifiers.org/hco/12/GRCh38#13218713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135363458-C-A

13218713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363458-C-T

13218762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363505-G-T

http://identifiers.org/hco/12/GRCh38#13218779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#135363522-C-A

13218779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363522-C-T

13218790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363533-G-T

13218792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363535-A-G

13218796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363539-G-T

13218887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363640-A-G

13218892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363645-A-T

13218919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363672-G-A

13218970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363720-G-A

13218970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135363720-G-T

13219858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135364153-C-G

13219901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3333
most severe consequence: 3 prime UTR variant
orthologous variants: 135364201-G-A