119212589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 122778149-G-T

119212738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122778010-G-T

119212742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 122778006-G-A

119212742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 122778006-G-C

119212742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 122778006-G-T

119212761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122777998-G-A

119212761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122777998-G-T

119213003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122777867-C-T

http://identifiers.org/hco/4/GRCh38#119213019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122777855-C-A

119213019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122777855-C-G

119213019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122777855-C-T

http://identifiers.org/hco/4/GRCh38#119213041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122777843-C-A

119213041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122777843-C-T

119213138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122777824-G-A

119213138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122777824-G-T

119213283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122777752-C-T

http://identifiers.org/hco/4/GRCh38#119213320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122777719-C-A

119213320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122777719-C-G

119213320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122777719-C-T

119213528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122777512-G-T

119213810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122777323-C-T

119214083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122777168-G-T

119214660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122776649-G-T

119214730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122776578-A-G

119215182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122776149-G-A

119215188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122776143-T-C

119215339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122775987-C-T

119215542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122775536-G-T

119215545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122775533-C-T

http://identifiers.org/hco/4/GRCh38#119217499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122773959-C-A

119217588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122773903-G-A

http://identifiers.org/hco/4/GRCh38#119217740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122773782-C-A

119217784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122773749-G-T

119217799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122773734-G-T

119217870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122773664-T-C

119217940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122773591-G-T

119217941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122773590-G-A

http://identifiers.org/hco/4/GRCh38#119227710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122772716-C-A

119227742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122772685-A-G

119227751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122772676-C-T

119227901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122772556-T-C

119228044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122772388-G-T

119228119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122772307-C-T

119228407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122772060-C-G

119228510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122771960-A-G

119228784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122771699-A-G

119228803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122771680-G-A

119229058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122771459-G-A

119230986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122769849-T-C

119231277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122769610-T-G

119231351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122769536-C-T

119231851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122769158-C-T

http://identifiers.org/hco/4/GRCh38#119232379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122768705-A-C

119232379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122768705-A-T

119232607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122768534-T-G

119232612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122768529-A-G

119232632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122768510-T-C

119232688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122768468-T-C

119233085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122768125-A-G

119233455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122767820-T-G

http://identifiers.org/hco/4/GRCh38#119233828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122766689-C-A

119233828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122766689-C-T

119233874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122766645-A-G

119235031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122764005-A-G

119235244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122763789-T-A

119238946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122763141-A-G

119239942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122762197-T-C

119240758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122761131-T-C

119240798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122761092-G-C

119241162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122760795-G-A

119241347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122760626-T-G

119241885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122760150-C-G

119242141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122759811-T-G

119242488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122759413-T-C

119242584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122759320-A-G

119242613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122759306-G-T

119243876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122759195-T-C

119243924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122759136-C-T

119243950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122759106-A-G

119244054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122759049-A-G

119244150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122758966-T-C

119244471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122758770-G-A

119244471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122758770-G-C

119244753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122758555-G-C

119244809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122758508-A-G

119245066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122758227-T-C

http://identifiers.org/hco/4/GRCh38#119245267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122758060-A-C

119245460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122757881-A-G

119245650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122757716-T-C

119245905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122757370-A-G

119248897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122756516-T-C

http://identifiers.org/hco/4/GRCh38#119249001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122756426-C-A

119249001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122756426-C-T

119249017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122756410-T-C

119249043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122756384-A-G

119249052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122756375-T-C

119249112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122756320-T-C

119256370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122754955-T-C

http://identifiers.org/hco/4/GRCh38#119256406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122754918-A-C

119256410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122754914-A-G

http://identifiers.org/hco/4/GRCh38#119256638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122754693-A-C

http://identifiers.org/hco/4/GRCh38#119256639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122754692-C-A

119256639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122754692-C-T

119256821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122754257-A-G

119256926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122754158-G-A

119256945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122754139-G-A

119257024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122754062-A-G

119258294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122753833-G-A

119258352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122753777-T-G

http://identifiers.org/hco/4/GRCh38#119259701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122752902-C-A

119259701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122752902-C-G

119259701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122752902-C-T

119259705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122752898-G-A

119259705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122752898-G-T

119259733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122752883-A-G

119259733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122752883-A-T

http://identifiers.org/hco/4/GRCh38#119259734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122752882-C-A

http://identifiers.org/hco/4/GRCh38#119259737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122752879-C-A

http://identifiers.org/hco/4/GRCh38#119259756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122752863-C-A

119259756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122752863-C-T

119259763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122752856-A-G

119259763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122752856-A-T

119259789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122752828-G-A

119259936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122752669-T-C

119259936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122752669-T-G

119260007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122752598-T-A

119260007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122752598-T-G

http://identifiers.org/hco/4/GRCh38#119260013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122752592-C-A

119260398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122751490-T-C

119260433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122751453-A-G

http://identifiers.org/hco/4/GRCh38#119260691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122751168-C-A

119260691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122751168-C-T

http://identifiers.org/hco/4/GRCh38#119260771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122751084-A-C

http://identifiers.org/hco/4/GRCh38#119260795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122751060-C-A

http://identifiers.org/hco/4/GRCh38#119260801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122751054-C-A

119261274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122750888-A-T

119261600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122750600-G-A

119261600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122750600-G-T

119261633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122750566-G-A

119261692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122750515-A-G

119261742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 122750468-G-A

119261742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 122750468-G-T

http://identifiers.org/hco/4/GRCh38#119261760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122750450-A-C

119261853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 122750357-A-G

http://identifiers.org/hco/4/GRCh38#119261945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122750279-C-A

119261946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122750278-A-T

119262260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122750134-C-T

119264832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122749656-A-G

119264904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122749578-A-G

119265148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122749350-T-G

119265241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122749266-C-G

119265297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122749201-A-G

119265983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122748785-A-G

119266008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122748761-C-G

http://identifiers.org/hco/4/GRCh38#119266153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122748618-C-A

119266153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122748618-C-T

119266174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122748598-A-G

119266180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122748592-T-C

119266242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122748527-C-T

119266324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 122748447-G-T

119266462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122748325-G-A

119266462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122748325-G-T

119266494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122748294-A-G

119266577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122748144-T-C

119266591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122748130-A-T

http://identifiers.org/hco/4/GRCh38#119267051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122747559-A-C

119267051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122747559-A-G

119267181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122747122-A-G

119267195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122747114-T-G

119267238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122747069-A-G

119267303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122747009-T-C

119267378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 122746931-T-C

119267378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 122746931-T-G

119267494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122746818-T-G

119267529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122746779-T-C

http://identifiers.org/hco/4/GRCh38#119267550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122746772-C-A

119267550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122746772-C-G

119267550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122746772-C-T

119267713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122746599-A-G

119267761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122746546-G-A

119267764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122746544-A-T

119267839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122746472-A-G

119267884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122746427-T-G

http://identifiers.org/hco/4/GRCh38#119268207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122746379-A-C

119268207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122746379-A-G

119268207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122746379-A-T

119268282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122746339-G-A

119268282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122746339-G-C

119268520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122746071-G-T

119268577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122746022-T-A

119269621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122745031-A-G

119269677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122744975-G-A

119269677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122744975-G-C

119269677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122744975-G-T

119269721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122744934-A-G

119269742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122744913-A-G

119269874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122744782-A-G

119270022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122744672-A-G

119270768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122744081-A-T

119270771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122744078-C-T

119271257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122743564-A-G

119271281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122743518-A-G

119271281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122743518-A-T

119271284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122743515-T-C

119271309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122743490-A-G

http://identifiers.org/hco/4/GRCh38#119271319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122743480-C-A

119271319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122743480-C-T

119271328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122743471-T-G

http://identifiers.org/hco/4/GRCh38#119271364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122743435-C-A

119271364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122743435-C-T

119271386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122743413-A-G

http://identifiers.org/hco/4/GRCh38#119271411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122743388-A-C

119271698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122743098-T-C

119271736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122743060-A-G

119271784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122743012-T-C

119271907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122742889-A-G

119272051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122742658-G-A

119272056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122742653-T-A

119272177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122742434-T-C

http://identifiers.org/hco/4/GRCh38#119272207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122742321-C-A

119272268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122742260-T-G

119272309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122742220-T-C

119272571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122742049-G-A

119272588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122742031-A-G

119272588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122742031-A-T

119272679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122741933-G-T

http://identifiers.org/hco/4/GRCh38#119272792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122741810-C-A

119272905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122741714-A-G

http://identifiers.org/hco/4/GRCh38#119273464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122741360-C-A

119273464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122741360-C-T

119273489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122741335-A-T

119273523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122741281-A-G

119273563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122741153-G-A

119273563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122741153-G-T

119273586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122741130-G-A

119273586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122741130-G-C

119273586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122741130-G-T

http://identifiers.org/hco/4/GRCh38#119273634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122741082-A-C

http://identifiers.org/hco/4/GRCh38#119273684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122741032-C-A

119273688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 122741028-A-G

119273741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122740970-T-A

119281220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122736521-A-T

119281404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122736375-G-A

http://identifiers.org/hco/4/GRCh38#119282211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122735624-C-A

119283276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122734714-A-G

119283672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122734472-T-C

119283987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122734186-G-A

119284036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122734139-G-C

http://identifiers.org/hco/4/GRCh38#119284115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122734076-A-C

119284115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122734076-A-G

119284153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122734049-T-A

119286217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122733521-G-T

http://identifiers.org/hco/4/GRCh38#119286329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122733302-A-C

119286744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122732878-A-G

119287655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122732543-A-G

http://identifiers.org/hco/4/GRCh38#119287832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122732256-A-C

119288013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122732098-T-G

119288064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122732026-A-G

119288218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122731908-A-G

http://identifiers.org/hco/4/GRCh38#119288257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122731853-A-C

119288461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122731644-G-A

119288461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122731644-G-T

119290717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122729971-C-T

http://identifiers.org/hco/4/GRCh38#119290871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122729865-A-C

119291093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122729788-A-G

http://identifiers.org/hco/4/GRCh38#119291163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122729733-A-C

119291163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, splice_acceptor_variant
orthologous variants: 122729733-A-G

119291163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant, splice_acceptor_variant
orthologous variants: 122729733-A-T

119291170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 122729726-A-G

119291170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 122729726-A-T

119291256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 122729640-A-G

119291272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122729605-T-C

119291272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122729605-T-G

119291307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122729576-G-T

119291310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122729573-T-C

119291368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122729529-G-T

119291395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122729502-T-C

119291439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122729455-C-T

119292038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122728608-T-A

119292578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 122728005-G-A

119292781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 122727796-T-C

119292826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 122727751-T-A

119292840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 122727737-G-C

119292858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 122727716-C-T

http://identifiers.org/hco/4/GRCh38#119292896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122727678-A-C

119292984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 122727596-C-T

119293000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 122727580-C-T

119293004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 122727576-C-G

119293004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 122727576-C-T

119293249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122727362-T-C

119293249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122727362-T-G

http://identifiers.org/hco/4/GRCh38#119293390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122727264-A-C

119293471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122727238-G-T

119293515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122727194-G-A

119293515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122727194-G-T

119293546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122727171-A-G

http://identifiers.org/hco/4/GRCh38#119293856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#122726895-C-A

119293856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122726895-C-T

119294183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122726608-C-T

119294558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122726305-G-T

119295346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29255
most severe consequence: 3 prime UTR variant
orthologous variants: 122725598-C-T