74289469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 5 prime UTR variant
orthologous variants: 134581125-T-C

http://identifiers.org/hco/7/GRCh38#74289475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134581119-C-A

74289475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 5 prime UTR variant
orthologous variants: 134581119-C-T

74289516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 134581078-C-T

http://identifiers.org/hco/7/GRCh38#74289564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#134581021-C-A

74289617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 134580997-C-T

74289633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 5 prime UTR variant
orthologous variants: 134580981-G-A

74289756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134580875-G-A

74289756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134580875-G-T

http://identifiers.org/hco/7/GRCh38#74289847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134580776-C-A

74289847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134580776-C-T

74289856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134580767-G-T

74289952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134580694-G-A

74290496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134580197-C-T

74290609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134580085-C-T

74290684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134579993-G-A

74290760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134579905-C-T

74290989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134579670-T-G

74291045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134579636-T-A

74291045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134579636-T-C

74291221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134579435-G-A

74291345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134579357-A-T

74291616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134579136-T-C

74291734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134579007-G-A

74291747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134579003-C-T

74291783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134578973-C-T

74291799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134578954-G-A

74291821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134578924-T-C

http://identifiers.org/hco/7/GRCh38#74291832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134578913-C-A

74291832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134578913-C-T

74292314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134578492-G-A

74292595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134578181-T-C

74292605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134578171-C-G

74292605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134578171-C-T

74292630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, undefined
orthologous variants: 134578126-C-T

74293141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134577099-C-G

74293141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134577099-C-T

74299592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134573458-G-T

74299629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134573425-C-T

74299635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134573419-C-T

74302723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134571098-T-C

74302768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134571055-G-A

74303078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134570735-C-T

74303125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134570689-G-A

74306428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134570096-C-T

74306482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134570030-C-T

74306557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134569929-G-A

74306619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134569869-G-A

74306873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, undefined
orthologous variants: 134569178-C-T

74307001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134569055-C-T

74317613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134563956-A-G

74317613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134563956-A-T

http://identifiers.org/hco/7/GRCh38#74317617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134563952-C-A

74317617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134563952-C-G

74317622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134563947-G-A

74317622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134563947-G-T

74317637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134563932-T-C

74325263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134559783-G-A

74325304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134559747-G-A

74325309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134559742-C-T

74328140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134557568-G-A

74328317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134557449-A-G

74328431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134557351-G-A

74328522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134557284-G-T

74328556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134557252-G-C

74328556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134557252-G-T

74328648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134557154-A-G

74332735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134554865-C-T

74332798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134554838-A-G

74332926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134554697-T-C

74334439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134552685-T-G

74334482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134552642-G-A

http://identifiers.org/hco/7/GRCh38#74338354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134552072-A-C

74338354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134552072-A-G

74338355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134552071-G-A

74338355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134552071-G-C

74338355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134552071-G-T

http://identifiers.org/hco/7/GRCh38#74338363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134552063-C-A

http://identifiers.org/hco/7/GRCh38#74338374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134552052-C-A

74338374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134552052-C-T

74338404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134552026-G-A

74338404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134552026-G-T

74338409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134552021-A-G

74338484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134551958-C-T

74338669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134551773-G-A

74338669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134551773-G-T

74338774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134551668-A-T

74338867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134551575-A-G

74338867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134551575-A-T

74338918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134551524-A-G

74338967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134551475-G-T

http://identifiers.org/hco/7/GRCh38#74339066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134551383-C-A

74339122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134551328-G-A

74339125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134551325-A-G

74339128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134551322-G-A

74339128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134551322-G-T

74339228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134551237-G-A

74353727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134546981-A-G

74354007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134546756-A-G

http://identifiers.org/hco/7/GRCh38#74354015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134546748-C-A

74354073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134546719-G-A

74354073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134546719-G-T

74354082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134546710-T-C

74354108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134546689-A-G

http://identifiers.org/hco/7/GRCh38#74354140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134546662-C-A

74354140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134546662-C-T

74356256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134546017-C-G

74356291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134545983-G-A

http://identifiers.org/hco/7/GRCh38#74356299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134545978-A-C

74356299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134545978-A-G

74356338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134545945-G-A

74356338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134545945-G-T

74356397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134545893-C-T

74356398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134545892-C-G

74356564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134545727-A-G

74356629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134545662-G-A

74356629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134545662-G-T

http://identifiers.org/hco/7/GRCh38#74356653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134545635-C-A

74356653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134545635-C-G

74356653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134545635-C-T

74356734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134545571-G-T

74356837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134545484-C-T

74357206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134545232-A-G

74357295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134545115-T-G

http://identifiers.org/hco/7/GRCh38#74357416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134544994-C-A

74357416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134544994-C-T

74357421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134544989-A-G

http://identifiers.org/hco/7/GRCh38#74360049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134543050-C-A

74360081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134543023-G-A

74360081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134543023-G-T

http://identifiers.org/hco/7/GRCh38#74360162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134542962-C-A

74360162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134542962-C-T

http://identifiers.org/hco/7/GRCh38#74360209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134542917-C-A

74360280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: splice donor variant
orthologous variants: 134542846-T-A

74360280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: splice donor variant
orthologous variants: 134542846-T-C

74360280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: splice donor variant
orthologous variants: 134542846-T-G

http://identifiers.org/hco/7/GRCh38#74360282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134542844-C-A

74360282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134542844-C-G

74360282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134542844-C-T

http://identifiers.org/hco/7/GRCh38#74360290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134542839-C-A

74360290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134542839-C-T

http://identifiers.org/hco/7/GRCh38#74360298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134542831-C-A

74360298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134542831-C-G

74360298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134542831-C-T

74360304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134542823-G-C

74362264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134541350-A-G

74363149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134540122-G-C

74363163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134540108-C-T

74363169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134540102-T-C

74363179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134540092-T-C

74363450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134539846-G-T

74363465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134539831-A-G

74364356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134538978-G-A

74364356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134538978-G-C

74364356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134538978-G-T

74364367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134538967-C-T

http://identifiers.org/hco/7/GRCh38#74364371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134538963-C-A

74364371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134538963-C-G

74364371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134538963-C-T

http://identifiers.org/hco/7/GRCh38#74364416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134538917-C-A

74364416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134538917-C-G

74364416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134538917-C-T

74364417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134538916-G-A

74364417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134538916-G-C

74364417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134538916-G-T

74365416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134536898-T-C

74365419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, undefined
orthologous variants: 134536895-C-T

74372288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134534697-G-A

74372300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134534675-G-A

74372353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134534626-T-C

74372611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134534037-G-A

74372633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134534013-G-A

74372674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134533981-C-T

74372689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134533964-T-A

74372689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134533964-T-C

http://identifiers.org/hco/7/GRCh38#74372691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134533962-A-C

74372705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134533949-C-T

http://identifiers.org/hco/7/GRCh38#74372855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134533781-C-A

74372855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134533781-C-T

74372863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134533773-T-G

74372884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134533753-T-A

74372884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134533753-T-C

74372884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134533753-T-G

74372995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, missense_variant
orthologous variants: 134533627-G-T

http://identifiers.org/hco/7/GRCh38#74373042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134533579-C-A

74373042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134533579-C-T

74375426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134532619-G-A

http://identifiers.org/hco/7/GRCh38#74375575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134532535-C-A

74375575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134532535-C-G

74375670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134532449-C-G

http://identifiers.org/hco/7/GRCh38#74375856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134532342-C-A

74375856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134532342-C-G

74375856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134532342-C-T

74376016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134532184-G-A

http://identifiers.org/hco/7/GRCh38#74376061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134532139-A-C

74376061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134532139-A-G

74376127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134532073-G-A

74376148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134532052-G-A

http://identifiers.org/hco/7/GRCh38#74376577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134531623-C-A

74376577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134531623-C-T

74376628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134531572-C-T

http://identifiers.org/hco/7/GRCh38#74376830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134531370-C-A

74376830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 134531370-C-T

http://identifiers.org/hco/7/GRCh38#74376904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134531303-C-A

74376946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134531273-T-A

74376946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134531273-T-C

74377018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134531220-G-C

74377504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134530694-G-A

74380291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134529733-G-A

74380291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134529733-G-C

74380415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134529622-T-C

74380593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134529171-G-A

74380593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134529171-G-C

74380593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134529171-G-T

http://identifiers.org/hco/7/GRCh38#74380781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134529025-C-A

74380781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134529025-C-G

http://identifiers.org/hco/7/GRCh38#74380937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#134528877-C-A

74380937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 134528877-C-T

74380959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 134528860-G-A

74381003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134528827-T-C

74381003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134528827-T-G

74381011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134528819-G-A

74381011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134528819-G-T

74381012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134528818-G-A

74381012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134528818-G-T

74386352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134527171-T-A

74386352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134527171-T-C

74386368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134527156-T-A

74386368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134527156-T-C

74386368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134527156-T-G

74386387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134527147-G-A

74386387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134527147-G-T

74386389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134527145-G-T

74386397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134527137-G-A

74386397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134527137-G-T

74386414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134527121-G-A

74386414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134527121-G-T

http://identifiers.org/hco/7/GRCh38#74386441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134527095-C-A

74386441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134527095-C-T

74386498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134527048-C-G

http://identifiers.org/hco/7/GRCh38#74386503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134527043-C-A

74386503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134527043-C-G

74386623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134526923-G-A

74386865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134526699-A-G

74386865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134526699-A-T

74386893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134526664-T-A

74386893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134526664-T-C

74386893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134526664-T-G

74386907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134526650-C-T

74386920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134526638-G-A

74386947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134526620-T-C

74386969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134526613-G-A

74389129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 134525211-G-A

74389129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: non_coding_transcript_exon_variant, stop_gained, synonymous_variant
orthologous variants: 134525211-G-T

74389263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134525077-A-G

74396940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134523333-T-C

74396948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134523325-A-G

74396948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134523325-A-T

http://identifiers.org/hco/7/GRCh38#74396965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134523304-A-C

74396965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134523304-A-G

74396992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134523278-G-A

74396992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134523278-G-T

74397062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134523226-C-T

74397090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134523204-C-T

74397317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134522987-G-A

74397320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134522984-G-T

74397568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134522745-G-C

74399882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521870-C-T

74399910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521842-T-A

74399926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521827-G-A

74400023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521709-T-C

74400026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521706-G-A

74400067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521616-A-T

74400118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521565-C-G

74400125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521558-A-G

74400125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521558-A-T

74400257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521342-G-A

74400257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521342-G-T

http://identifiers.org/hco/7/GRCh38#74400265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134521336-C-A

74400265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521336-C-T

74400294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521307-T-A

74400294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521307-T-C

http://identifiers.org/hco/7/GRCh38#74400324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134521298-C-A

74400324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521298-C-G

http://identifiers.org/hco/7/GRCh38#74400328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134521294-C-A

74400391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134521235-G-A

74400391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134521235-G-C

74400391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134521235-G-T

http://identifiers.org/hco/7/GRCh38#74400409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134521217-C-A

74400409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134521217-C-G

74400409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134521217-C-T

74400472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134521154-G-A

74400472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: missense variant
orthologous variants: 134521154-G-T

74400558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134521068-G-A

http://identifiers.org/hco/7/GRCh38#74400600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134521056-C-A

74401489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134520830-C-T

74401492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron_variant, undefined
orthologous variants: 134520827-C-G

74401732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134520572-T-G

http://identifiers.org/hco/7/GRCh38#74401769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134520534-C-A

http://identifiers.org/hco/7/GRCh38#74403715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134519740-C-A

74403715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134519740-C-T

http://identifiers.org/hco/7/GRCh38#74403759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134519715-C-A

74403759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134519715-C-T

74403783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134519695-T-C

74403786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134519692-C-T

74403797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134519681-C-T

74403798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: intron variant
orthologous variants: 134519680-T-C

http://identifiers.org/hco/7/GRCh38#74403870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134519612-C-A

74403928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134519553-A-T

http://identifiers.org/hco/7/GRCh38#74403985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134519496-C-A

74403985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134519496-C-T

http://identifiers.org/hco/7/GRCh38#74404040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134519434-C-A

74404040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134519434-C-T

74404120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134519363-A-G

74404150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134519337-C-T

74404186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134519299-C-G

74404186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134519299-C-T

http://identifiers.org/hco/7/GRCh38#74404235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134519243-C-A

74404235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134519243-C-T

74404265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134519216-G-A

74404265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134519216-G-T

http://identifiers.org/hco/7/GRCh38#74404511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134519056-A-C

74404511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134519056-A-G

http://identifiers.org/hco/7/GRCh38#74404516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134519052-C-A

74404516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134519052-C-G

74404516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134519052-C-T

http://identifiers.org/hco/7/GRCh38#74404526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134519039-C-A

74404526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134519039-C-T

74404605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134518968-T-C

http://identifiers.org/hco/7/GRCh38#74404613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134518960-C-A

74405332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134518801-G-T

http://identifiers.org/hco/7/GRCh38#74405381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#134518766-C-A

74405382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134518765-A-G

74405408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134518738-A-G

74405424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134518722-T-C

74405438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134518708-T-C

74405452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134518694-G-T

http://identifiers.org/hco/7/GRCh38#74405523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134518630-C-A

74405523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134518630-C-T

74405554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134518604-G-A

74405591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134518567-G-A

74405629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134518528-T-C

74405826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134518346-G-A

74405826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134518346-G-T

http://identifiers.org/hco/7/GRCh38#74405841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134518329-C-A

74405841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134518329-C-T

74405860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134518311-T-C

http://identifiers.org/hco/7/GRCh38#74405868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#134518303-C-A

74405868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2586
most severe consequence: 3 prime UTR variant
orthologous variants: 134518303-C-T