http://identifiers.org/hco/1/GRCh38#36339742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126034658-C-A

36339742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034658-C-T

36339762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034641-G-C

36339762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034641-G-T

36339794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034612-T-C

36339813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034593-A-G

http://identifiers.org/hco/1/GRCh38#36339985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126034442-C-A

36340011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034416-G-A

36340042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034387-G-A

36340042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034387-G-C

36340042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034387-G-T

36340076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034350-A-G

36340076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034350-A-T

http://identifiers.org/hco/1/GRCh38#36340115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126034318-C-A

36340115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034318-C-G

36340115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034318-C-T

36340119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034313-G-A

36340119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126034313-G-T

http://identifiers.org/hco/1/GRCh38#36340414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126034022-C-A

36340531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033912-G-A

36340531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033912-G-T

36340535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033908-C-T

36340766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033682-G-A

36340766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033682-G-T

36340916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033575-T-C

36341060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033474-A-G

36341098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033434-T-C

36341098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033434-T-G

36341134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033407-G-A

36341134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033407-G-T

http://identifiers.org/hco/1/GRCh38#36341138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126033403-C-A

36341138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033403-C-T

36341216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033333-G-A

36341216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033333-G-T

36341273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033284-G-T

36341434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033153-G-T

36341438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033149-A-T

http://identifiers.org/hco/1/GRCh38#36341454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126033132-C-A

36341454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126033132-C-G

http://identifiers.org/hco/1/GRCh38#36341585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126032999-C-A

http://identifiers.org/hco/1/GRCh38#36341680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126032900-C-A

36341680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3 prime UTR variant
orthologous variants: 126032900-C-T

36341834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 126032740-A-G

36341927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 126032647-A-T

36342085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032522-C-T

36342099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032509-C-T

36342102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032506-A-G

36342135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032458-G-T

36342147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032446-G-A

36342147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032446-G-C

36342416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032214-A-G

http://identifiers.org/hco/1/GRCh38#36342429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126032203-C-A

36342429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032203-C-G

36342434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032198-G-T

36342520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032132-C-T

36342531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032121-T-C

36342531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032121-T-G

http://identifiers.org/hco/1/GRCh38#36342585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126032080-C-A

36342585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032080-C-G

36342585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032080-C-T

36342600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032068-C-T

36342614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126032054-A-G

36342888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 126031966-C-T

http://identifiers.org/hco/1/GRCh38#36342935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126031919-C-A

36342935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126031919-C-T

36342943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126031911-T-C

http://identifiers.org/hco/1/GRCh38#36342972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#126031884-A-C

36343060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126031792-A-T

36343092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126031751-A-G

36343092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126031751-A-T

http://identifiers.org/hco/1/GRCh38#36343248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126031668-A-C

36343379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: synonymous variant
orthologous variants: 126031621-C-T

36343495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126031513-C-T

36343552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126031474-A-G

36343565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126031461-G-T

36343817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126031020-T-C

36343984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 126030864-G-A

36344003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126030847-G-A

36344014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126030825-G-A

http://identifiers.org/hco/1/GRCh38#36344040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126030796-C-A

36344040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126030796-C-G

36344040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126030796-C-T

36344080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126030750-G-T

36344258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: missense variant
orthologous variants: 126030567-G-A

36344258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: missense variant
orthologous variants: 126030567-G-T

36344311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126030517-G-A

36344311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126030517-G-T

36344629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126030222-G-A

36344634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126030217-C-T

36348633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126028954-T-C

36348651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126028936-G-A

36348651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126028936-G-T

http://identifiers.org/hco/1/GRCh38#36348691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126028927-C-A

36348691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126028927-C-T

36348726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: missense variant
orthologous variants: 126028892-G-A

http://identifiers.org/hco/1/GRCh38#36348967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126028663-C-A

36348967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126028663-C-T

http://identifiers.org/hco/1/GRCh38#36349585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126026985-C-A

36349664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126026892-C-T

36349845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126026774-T-C

36349928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126026730-G-A

36350192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126026462-G-A

36350360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126026329-T-C

36350393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126026309-G-A

36350481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126026210-C-T

36350497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126026189-C-T

36350817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126025990-T-C

36350914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126025926-C-T

36351039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126025792-G-A

36351601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126025459-G-A

36351973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126025139-C-T

36352076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126024884-T-C

36352164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126024823-G-A

36352511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126024525-G-C

36352592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126024444-T-C

36352937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126024155-C-T

36353042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126024094-A-G

36353310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126023864-A-G

36353352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126023821-T-G

36354230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126023645-C-T

36354255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126023622-G-T

36354309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126023589-T-C

36354336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126023569-T-A

36354336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126023569-T-C

36354342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126023563-G-A

36354517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126023395-A-G

36354682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126023302-G-A

36354682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126023302-G-C

36354682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126023302-G-T

http://identifiers.org/hco/1/GRCh38#36355107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126022929-C-A

http://identifiers.org/hco/1/GRCh38#36355112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126022924-C-A

36355112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron variant
orthologous variants: 126022924-C-T

36355276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126022767-T-C

36355493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126022578-G-T

36355499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126022571-G-A

36355499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126022571-G-T

36355726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126022418-G-A

36355745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126022399-C-G

36355745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126022399-C-T

http://identifiers.org/hco/1/GRCh38#36355767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126022377-C-A

36355787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126022360-G-A

36356933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126020351-G-T

http://identifiers.org/hco/1/GRCh38#36357003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126020302-C-A

36357003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126020302-C-T

36357897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126019918-G-A

36357904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126019911-C-T

36358639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126019047-T-C

36358843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 126018853-G-A

36359007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126018765-A-G

36361394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126017453-T-C

36361395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126017452-G-T

36361428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126017428-G-A

http://identifiers.org/hco/1/GRCh38#36361451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126017408-C-A

36361451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126017408-C-T

http://identifiers.org/hco/1/GRCh38#36361467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126017397-C-A

36361473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126017390-G-A

36361473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126017390-G-T

36361535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126017327-T-C

http://identifiers.org/hco/1/GRCh38#36361765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126017138-C-A

36361841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126017056-G-A

36365964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 126012818-C-T

36366576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126012264-C-T

http://identifiers.org/hco/1/GRCh38#36366760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126012073-C-A

36366760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126012073-C-G

http://identifiers.org/hco/1/GRCh38#36367295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126011875-C-A

36367391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126011785-G-A

36367473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126011535-G-A

http://identifiers.org/hco/1/GRCh38#36367921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126009606-C-A

36368005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126009525-G-A

36368005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126009525-G-T

36368096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126009434-A-G

36368121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126009414-T-C

36368123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126009412-T-C

http://identifiers.org/hco/1/GRCh38#36368164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126009386-C-A

36368170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126009380-G-A

36368928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126008271-G-A

36368980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126008226-T-C

36368997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126008208-A-G

36369005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126008200-T-C

http://identifiers.org/hco/1/GRCh38#36369023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#126008182-C-A

36369373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126007846-G-A

http://identifiers.org/hco/1/GRCh38#36369467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126007752-C-A

36369539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126007684-A-G

36369545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126007678-C-T

36369603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126007617-T-C

36369912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126007175-A-G

36370293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126006605-C-T

36374427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126004458-C-T

36375037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126003880-A-G

36377284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126003455-C-T

36377317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126003417-G-C

36377516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126003236-G-A

36377516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126003236-G-T

36377590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126003114-G-A

36378252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126002405-C-T

36378844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126002121-C-T

36378893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126002073-G-C

36378987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126001993-G-A

36378987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126001993-G-C

36379197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126001798-G-A

36379309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126001733-G-T

36381841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126000889-C-T

36382067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126000690-C-T

36382153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126000585-A-G

36382777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126000033-C-T

36383479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125999709-C-G

36383479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125999709-C-T

36383619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125999597-A-G

36383717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125999504-A-G

http://identifiers.org/hco/1/GRCh38#36383749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#125999466-C-A

36383832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125999407-C-T

36384143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125999308-C-T

36384328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125999251-C-G

36384329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125999250-C-T

36384404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125999176-T-C

http://identifiers.org/hco/1/GRCh38#36385841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#125997820-C-A

36385841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125997820-C-G

36385841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125997820-C-T

http://identifiers.org/hco/1/GRCh38#36385868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#125997793-C-A

36385868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125997793-C-G

36385868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21373
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125997793-C-T