67952066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: 11063706-G-A

http://identifiers.org/hco/8/GRCh38#67952099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#11063736-C-A

67952099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 11063736-C-G

http://identifiers.org/hco/8/GRCh38#67952105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#11063742-C-A

67952105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 11063742-C-T

http://identifiers.org/hco/8/GRCh38#67952121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11063758-A-C

67952121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: 11063758-A-G

http://identifiers.org/hco/8/GRCh38#67952152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11063774-C-A

67952152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: 11063774-C-T

67952157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: 11063779-G-A

67952157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: 11063779-G-T

http://identifiers.org/hco/8/GRCh38#67952168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11063791-C-A

http://identifiers.org/hco/8/GRCh38#67952190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11063822-C-A

67952190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: 11063822-C-T

http://identifiers.org/hco/8/GRCh38#67952205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11063837-C-A

67952205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: 11063837-C-G

67952205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: 11063837-C-T

67952248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: 11063882-T-C

http://identifiers.org/hco/8/GRCh38#67952274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11063908-C-A

67952274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: 11063908-C-T

67952293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: 11063927-G-T

http://identifiers.org/hco/8/GRCh38#67952300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11063934-C-A

67952300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: 5 prime UTR variant
orthologous variants: 11063934-C-G

http://identifiers.org/hco/8/GRCh38#67952427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11064025-C-A

67952427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11064025-C-G

67952427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11064025-C-T

67952584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11064155-C-G

67952584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11064155-C-T

67952645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11064199-G-A

67952717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11064240-T-C

67952749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11064268-G-A

67952749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11064268-G-C

67952749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11064268-G-T

67952766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11064284-A-G

67953142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11064626-C-T

67953248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11064719-G-A

67953312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11064798-T-A

67953853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11065327-A-G

67953854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11065328-T-C

67954384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11066382-A-G

67954391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11066389-T-A

67954460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11066459-T-G

67954556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11066555-A-G

67955553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11067409-A-T

67955692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11067530-G-A

67955696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11067534-G-A

67955698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11067536-A-G

67955860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11067644-A-G

http://identifiers.org/hco/8/GRCh38#67956045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11067731-A-C

67956232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11067909-C-T

67956387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11068101-A-G

67956532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11068251-A-G

67956646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11068355-G-A

http://identifiers.org/hco/8/GRCh38#67957090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11068776-C-A

67957177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11068870-G-T

http://identifiers.org/hco/8/GRCh38#67957214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11068915-C-A

67957214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11068915-C-G

67957355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069262-A-G

67957550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069430-A-G

http://identifiers.org/hco/8/GRCh38#67957686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11069534-C-A

http://identifiers.org/hco/8/GRCh38#67957806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11069639-C-A

67957884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069714-G-A

67957911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069743-G-A

67957950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069778-G-A

67957955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069783-G-A

67957975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069803-T-G

67958208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11070040-A-G

67958222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11070049-C-T

67958717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11070512-T-C

http://identifiers.org/hco/8/GRCh38#67958939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11070728-A-C

67959019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11070800-C-G

67959041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11070825-A-G

67959089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11070875-T-A

67959342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11071081-C-T

67960575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11072055-G-A

67960575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11072055-G-C

67960586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11072066-G-C

67960845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11072323-G-C

67961588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11074412-G-T

67961648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11074474-C-T

http://identifiers.org/hco/8/GRCh38#67961970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11074836-C-A

67961970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11074836-C-T

67962073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11074943-C-G

67962255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11075109-T-C

http://identifiers.org/hco/8/GRCh38#67962324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11075178-C-A

67962324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11075178-C-G

67962453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11075298-C-T

67962483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11075328-G-A

67963421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11075931-A-G

67963463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11075971-C-G

67963466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11075974-G-A

67963777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11076460-A-G

67963929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11076580-A-G

67963992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11076647-A-G

67964037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11076689-T-C

67964088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11076739-A-T

67964323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11076965-G-A

67965220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11078102-C-G

67965302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11078184-A-G

67965509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11078337-G-A

67965670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11078432-C-T

67965722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11078487-G-A

67965729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11078495-G-C

67965729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11078495-G-T

67965816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11078569-A-G

67966210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11079298-G-C

67966287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11079372-T-A

67966376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11079460-A-G

http://identifiers.org/hco/8/GRCh38#67966457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11079536-C-A

67967463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11080702-G-T

67967603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11080832-G-A

67967606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11080835-G-C

67967712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11080939-C-T

67967729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11080955-G-T

67968068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11080997-T-A

67968089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11081018-A-G

67968104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11081033-C-T

67968474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11081381-T-C

67968593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11081504-G-A

http://identifiers.org/hco/8/GRCh38#67968687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#11081598-A-C

67968687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11081598-A-G

67968687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11081598-A-T

67968707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11081618-A-G

67968755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11081666-T-A

67969097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11081981-A-G

67969131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11082014-G-A

67969152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11082037-T-A

67969392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11082289-C-G

67969515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11082418-A-G

http://identifiers.org/hco/8/GRCh38#67969814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11082711-A-C

67969859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11082755-T-G

67969890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11082782-T-C

67970173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11083018-G-T

67970280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11083093-C-T

67970412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11083226-A-T

67970629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11083442-T-A

67971262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11084686-T-C

67971390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11084788-T-C

67971418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11084817-T-C

67971604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11088967-A-T

http://identifiers.org/hco/8/GRCh38#67971632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11088992-A-C

67972084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11089423-G-A

67972171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11089510-G-A

67972526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11089871-C-G

67972526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11089871-C-T

67973420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11091820-A-G

67973892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11092235-A-G

67974173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11092520-A-G

67974377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11093036-G-A

67974484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11093148-A-G

67974544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11093209-G-T

67974746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11093413-A-G

http://identifiers.org/hco/8/GRCh38#67975045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11093685-C-A

67975078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11093717-C-T

http://identifiers.org/hco/8/GRCh38#67978327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11094178-C-A

67978454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11094307-A-G

67978520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11094448-G-A

67978520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11094448-G-C

67978880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11094790-T-C

67981521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11097072-T-C

67981536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11097088-A-G

67981710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11097244-G-A

67981761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11097289-G-T

http://identifiers.org/hco/8/GRCh38#67982015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11097548-C-A

67982015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11097548-C-T

67982534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11098062-T-C

67982675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11098190-G-A

67982675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11098190-G-T

67982709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11098224-T-G

67982725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11098238-C-T

67982844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11098342-A-G

67983025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11098532-T-C

67983035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11098543-C-G

67983047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11098555-A-T

http://identifiers.org/hco/8/GRCh38#67983333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11098849-A-C

http://identifiers.org/hco/8/GRCh38#67983339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11098855-C-A

67983621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099222-C-G

67983621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099222-C-T

67983736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099316-G-A

67983762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099335-T-C

67983762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099335-T-G

67983783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099351-C-T

67983795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099363-G-T

67984074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099598-A-G

67984138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099651-A-G

67984540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11103457-A-G

67984626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11103529-T-C

67984953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11103834-C-G

67985063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11103932-G-A

67985125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11103993-T-C

http://identifiers.org/hco/8/GRCh38#67985215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11104083-A-C

http://identifiers.org/hco/8/GRCh38#67985462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11104321-C-A

67985501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104363-G-A

67985783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104626-C-T

67985807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104655-G-T

67985850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104694-A-G

67985923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104772-T-C

67985935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104784-C-T

http://identifiers.org/hco/8/GRCh38#67989394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11105985-A-C

67989394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11105985-A-G

67989569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11106173-T-A

67989614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11106208-C-G

67989714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11106306-T-C

67989840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11106421-A-G

67989980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11106559-C-G

67992018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11107549-G-A

67992028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11107559-G-T

67992091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11107592-C-G

67992180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11107701-C-T

67992244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11107776-A-G

http://identifiers.org/hco/8/GRCh38#67992401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11107881-A-C

67993149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11108655-T-A

67993164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11108671-G-A

67993192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11108694-A-G

68002819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11113609-A-T

68002879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11113668-A-G

68002898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11113687-A-G

68002989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11113784-G-C

68003515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11114920-G-T

68007066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11115682-G-T

68007306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11115896-C-T

68007599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11116217-G-A

68007599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11116217-G-T

68008201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11116742-G-A

68009115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11117257-G-A

68012497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11124034-A-G

68012574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11124110-A-G

68012590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11124131-G-A

68012844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11124410-T-A

68012905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11124453-T-C

68013074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11124614-G-A

68013562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127093-A-G

68013666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127217-C-T

68013790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127327-T-C

68013792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127329-T-A

68013917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127445-C-T

68013927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127455-G-A

68013927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127455-G-C

68014037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127558-A-T

68014116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127631-C-G

68014219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127727-C-T

68014345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127875-A-G

68014390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127916-A-G

68014462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127975-A-G

68014641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11128119-G-A

68014703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11128178-G-A

68014806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11128279-C-T

68014888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11128349-G-C

http://identifiers.org/hco/8/GRCh38#68014911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11128376-A-C

68015135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11128590-T-C

68015357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11128778-C-T

68015411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11128824-A-G

68015419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11128832-A-G

68015462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11128875-A-G

68015526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11128939-C-T

68015643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11129054-G-A

68015686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11129088-C-T

68015767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11129168-C-T

68015801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11129184-T-C

http://identifiers.org/hco/8/GRCh38#68015834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11129215-C-A

68015913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11129335-A-T

68016025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11129438-A-T

68016058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11129472-A-G

68016224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11129643-G-A

68016547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11130016-T-G

68017096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11130509-C-G

68017213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11130651-G-A

68017213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11130651-G-T

http://identifiers.org/hco/8/GRCh38#68017250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11130745-C-A

http://identifiers.org/hco/8/GRCh38#68017268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11130763-A-C

http://identifiers.org/hco/8/GRCh38#68017365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11130864-A-C

68017365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11130864-A-G

68017385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11130906-C-T

68017390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11130911-A-G

68017419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11130938-A-G

68017424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11130942-T-C

68017434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11130952-A-G

68017448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11130999-A-G

68017530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11131095-G-A

68017580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11131144-C-T

http://identifiers.org/hco/8/GRCh38#68017719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11131284-C-A

http://identifiers.org/hco/8/GRCh38#68017727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11131292-C-A

68017727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11131292-C-G

68017727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11131292-C-T

http://identifiers.org/hco/8/GRCh38#68017734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11131299-A-C

68017734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11131299-A-G

68017734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11131299-A-T

http://identifiers.org/hco/8/GRCh38#68017767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11131469-A-C

68017767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11131469-A-T

68017869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11131573-G-C

68017869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11131573-G-T

68017902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11131606-A-G

68017902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11131606-A-T

68017951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11131655-T-A

68017951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11131655-T-G

68017966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11131670-T-A

68018007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11131712-G-C

68018007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11131712-G-T

68018154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11131847-T-C

68018172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11131865-G-A

68019397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11135856-G-A

68019397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11135856-G-T

68019451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11135909-A-G

68019451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11135909-A-T

68019460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11135916-T-G

http://identifiers.org/hco/8/GRCh38#68019505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11135968-A-C

68019679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11136148-A-T

68019725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11136190-T-C

68019725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11136190-T-G

68019807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11136325-A-G

68019910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11136430-G-A

68019910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11136430-G-C

68019910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11136430-G-T

68020122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11136649-C-T

68020127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11136654-A-G

68020153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11136680-G-A

68020153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11136680-G-C

http://identifiers.org/hco/8/GRCh38#68020604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11137071-C-A

68020640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11137108-G-A

68020640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11137108-G-C

68020770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11137228-T-C

68020854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11137311-C-T

68021145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11137600-A-G

68021365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11137788-T-G

68021519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11137933-A-G

http://identifiers.org/hco/8/GRCh38#68022225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11138410-A-C

68022225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11138410-A-G

68022225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11138410-A-T

68022395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11138572-G-A

68022398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11138575-C-T

68022455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11138628-T-G

68022470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11138644-G-T

http://identifiers.org/hco/8/GRCh38#68022638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11138782-A-C

68022750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11138861-G-A

68022922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11139069-T-C

68023150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11139339-G-A

68023487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11139629-G-T

68023561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11139703-T-C

68025996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11148940-T-G

68026063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11149005-G-A

68026144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11149020-G-A

68026144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11149020-G-C

68026154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11149030-T-C

68026163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11149039-T-A

68026227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11149079-T-C

68026228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11149080-G-C

68026583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11149411-A-G

http://identifiers.org/hco/8/GRCh38#68026717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11149559-A-C

68026717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11149559-A-G

68026807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11149642-G-A

68026918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11149948-A-G

68026972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150028-T-C

68027122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150149-G-A

68027122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150149-G-T

68027153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150181-A-G

68027153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150181-A-T

68027156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150186-G-A

68027156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150186-G-T

http://identifiers.org/hco/8/GRCh38#68027216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11150241-C-A

68027216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11150241-C-T

http://identifiers.org/hco/8/GRCh38#68027351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11150365-C-A

68027351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150365-C-T

http://identifiers.org/hco/8/GRCh38#68027357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11150374-C-A

68027389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150404-T-A

68027397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150412-T-A

68027397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150412-T-C

68027432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150456-G-T

68027436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150460-A-G

68027436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150460-A-T

68027446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150470-G-A

68027446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150470-G-T

68027619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150641-G-A

68027626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150648-T-C

68028672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11158292-T-C

68028729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11158352-T-C

68028735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11158358-C-G

68028963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11158608-C-T

68029099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11158729-G-A

68029099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11158729-G-C

68029163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11158789-A-G

http://identifiers.org/hco/8/GRCh38#68029626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11159210-C-A

http://identifiers.org/hco/8/GRCh38#68030425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11159877-C-A

68030425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11159877-C-T

http://identifiers.org/hco/8/GRCh38#68030439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11159885-C-A

68030439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11159885-C-T

http://identifiers.org/hco/8/GRCh38#68030449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11159895-C-A

68030489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11159933-A-G

http://identifiers.org/hco/8/GRCh38#68030690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11160134-A-C

68030708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11160161-G-A

68030731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11160190-T-C

68030769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11160223-C-T

68030786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11160240-A-G

http://identifiers.org/hco/8/GRCh38#68031273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11160733-A-C

68031273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11160733-A-G

68031500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11160944-C-T

http://identifiers.org/hco/8/GRCh38#68031975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11161396-A-C

68031988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11161409-A-G

68032729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11162730-A-G

68032729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11162730-A-T

68032752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11162751-A-G

68032770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11162768-T-G

68032803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11162779-A-T

68032811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11162787-C-G

68032811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11162787-C-T

68032820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11162798-G-A

68032863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11162842-C-G

68032863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11162842-C-T

http://identifiers.org/hco/8/GRCh38#68033032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11162999-A-C

68033032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11162999-A-T

68033557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11165024-C-T

68034103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11166197-G-A

68034209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11166301-T-A

68034240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11166331-A-G

68034333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11166478-G-C

68037140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11167418-A-T

68037296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11167564-C-T

68037300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11167568-C-T

68037396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11167663-A-G

68038150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168678-C-T

68038269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11168797-G-A

68038309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168836-G-A

68038309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168836-G-T

68038352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168881-G-A

68038352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168881-G-T

http://identifiers.org/hco/8/GRCh38#68038358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11168887-C-A

68038462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168931-G-T

68038525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168990-G-A

68038548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169013-A-G

68038640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169075-C-T

68038693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169127-T-C

68038883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169260-C-T

68038937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169296-C-G

68038998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169356-A-G

68042014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169754-A-G

68042047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169785-G-A

68044075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11170036-A-G

68044103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11170119-G-C

68044194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11170204-C-T

68044470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11171273-T-C

68044499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11171300-C-G

68044499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11171300-C-T

68044521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11171322-C-T

http://identifiers.org/hco/8/GRCh38#68044676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11171420-C-A

68044676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11171420-C-T

68044711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11171455-G-T

68044777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11171521-G-A

68044857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11171621-G-A

68045155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11171888-T-C

http://identifiers.org/hco/8/GRCh38#68045256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11171993-C-A

68045292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11172028-T-C

68046905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11172833-T-A

68047035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11172963-G-C

68047483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11173276-A-G

http://identifiers.org/hco/8/GRCh38#68047544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11173327-C-A

68047544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11173327-C-T

68047553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11173336-T-G

68047846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11173536-G-T

68048128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11173830-A-G

68048144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11173846-C-T

68048242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11173941-T-A

68048379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11174030-G-C

68048466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11174110-G-A

http://identifiers.org/hco/8/GRCh38#68048471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11174115-A-C

http://identifiers.org/hco/8/GRCh38#68049157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11174987-C-A

68049157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11174987-C-T

68049266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11175096-G-C

http://identifiers.org/hco/8/GRCh38#68049271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11175101-C-A

68049272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11175102-C-G

68049323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11175151-C-T

68049331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11175159-A-G

68049428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11175257-A-T

68049645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11175474-T-C

68049694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11175531-A-G

68049768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11175605-T-G

68049945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11175870-G-A

68050137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11176031-A-G

68051380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11176537-A-G

68051399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11176554-C-T

68051515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11176598-G-A

68051741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11176795-A-G

68051978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11176987-A-G

http://identifiers.org/hco/8/GRCh38#68052236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11177191-C-A

68052272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11177224-A-G

68052341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11177285-T-G

68052369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11177303-G-T

68052479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11177375-T-A

68052480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11177376-A-G

http://identifiers.org/hco/8/GRCh38#68052652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11177422-C-A

68052768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11177543-C-T

http://identifiers.org/hco/8/GRCh38#68052782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11177557-C-A

68052853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11177622-T-A

68052867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11177636-A-G

68053054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11177784-T-C

68053054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11177784-T-G

68053107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11177837-T-C

68053182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11177912-A-T

68053188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11177918-A-T

68053206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11177936-A-G

68053233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11177963-A-G

68053269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11177999-G-A

68053269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11177999-G-C

68053296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178026-G-A

http://identifiers.org/hco/8/GRCh38#68053311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11178041-A-C

68053311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178041-A-G

68053321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178054-A-G

68053329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178062-A-G

68053578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178760-T-C

68053792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178976-A-G

68054650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11179471-C-T

68054665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11179486-G-C

http://identifiers.org/hco/8/GRCh38#68054666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11179487-C-A

68054748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11179564-C-T

68054800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11179602-A-G

http://identifiers.org/hco/8/GRCh38#68054882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11179666-A-C

68054958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11179746-T-C

68055067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11179851-A-G

68055347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180112-A-G

68055437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180185-G-A

68055438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180186-T-G

68055624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180304-G-C

68055668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180351-C-T

68055690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180372-G-C

68055690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180372-G-T

68055709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180391-C-G

http://identifiers.org/hco/8/GRCh38#68055728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11180410-C-A

68055728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180410-C-T

68055737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180419-G-A

http://identifiers.org/hco/8/GRCh38#68055739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11180422-C-A

68055749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180432-A-T

68055750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180433-T-A

68055751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180434-G-A

68055751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180434-G-T

http://identifiers.org/hco/8/GRCh38#68055752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11180435-C-A

68055752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180435-C-G

68055765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180448-G-C

http://identifiers.org/hco/8/GRCh38#68055766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11180449-C-A

68055766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180449-C-T

68055782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180465-G-T

68055825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11180501-G-A

68055873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11180549-T-C

68055933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11180609-A-G

68055933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11180609-A-T

http://identifiers.org/hco/8/GRCh38#68056102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11180744-C-A

68056194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180840-T-C

68056284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180920-C-G

68056284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180920-C-T

68056338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180969-C-T

http://identifiers.org/hco/8/GRCh38#68056347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11180981-A-C

68056585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11181124-G-A

http://identifiers.org/hco/8/GRCh38#68056634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11181167-C-A

http://identifiers.org/hco/8/GRCh38#68058190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11181875-C-A

68058222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11181901-G-C

http://identifiers.org/hco/8/GRCh38#68058372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11182041-C-A

68058378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182047-G-C

68058426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182087-T-C

http://identifiers.org/hco/8/GRCh38#68058428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11182089-A-C

68058781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182139-T-G

68059002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182362-T-C

68059020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182382-T-A

68059175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182532-C-T

68059223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182581-T-C

68059283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182642-A-G

http://identifiers.org/hco/8/GRCh38#68060527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11182816-C-A

68060527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182816-C-T

68060551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182842-A-G

68060593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182885-A-G

http://identifiers.org/hco/8/GRCh38#68060603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11182895-C-A

68060603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182895-C-T

http://identifiers.org/hco/8/GRCh38#68060608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11182899-C-A

68060608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182899-C-T

68060610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182901-G-A

68060613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11182904-T-G

68060724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11183012-T-C

68060733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11183021-C-T

68060751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11183039-A-G

68060752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11183040-T-C

68060806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11183092-T-C

68060919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11183199-T-A

68060919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11183199-T-C

68060919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11183199-T-G

68061339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11183573-T-C

68061344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11183587-G-A

68061622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11183845-T-C

68061760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11183934-C-T

68062310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11184298-T-C

68062319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11184307-G-A

68062594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11184568-T-C

http://identifiers.org/hco/8/GRCh38#68062620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11184593-C-A

68062651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11184626-T-A

68062737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11184710-T-G

68062761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11184757-G-T

68062774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11184814-A-G

68062833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11184993-T-C

http://identifiers.org/hco/8/GRCh38#68062968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11185127-A-C

68062988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11185151-T-C

68063045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11185178-T-G

http://identifiers.org/hco/8/GRCh38#68063860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11187519-A-C

68063879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11187538-T-C

68063992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11187686-A-G

68064085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11187784-G-A

68064085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11187784-G-T

68064941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11188250-G-T

68065018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11188315-C-G

68065228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11188470-T-C

68065390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11189042-T-G

68065724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11189388-T-A

68065724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11189388-T-C

68065801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11189466-A-G

68065815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11189480-A-G

68068375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11192489-A-G

68068455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11192572-T-C

68068543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11192664-C-G

68068625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11192784-T-C

68068789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193139-A-G

http://identifiers.org/hco/8/GRCh38#68068910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11193260-A-C

68068910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193260-A-G

68068910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193260-A-T

http://identifiers.org/hco/8/GRCh38#68068949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11193282-A-C

68068949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193282-A-G

68068949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193282-A-T

68068955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193288-A-G

68068956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193289-T-C

68068966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193299-T-G

68068968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193301-A-G

68069189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193499-T-C

68069254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193539-A-T

http://identifiers.org/hco/8/GRCh38#68069421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11193635-C-A

68069492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193707-T-C

68069535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193747-G-C

68069665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193870-A-G

http://identifiers.org/hco/8/GRCh38#68069685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11193887-A-C

68069708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193911-T-A

68069708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193911-T-G

68069734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193937-T-A

68069734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193937-T-C

68069734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193937-T-G

68069737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193940-T-A

68069737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193940-T-C

68069737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193940-T-G

68069763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193966-T-C

68069764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193967-T-C

68069764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193967-T-G

68069801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194004-T-A

68069801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194004-T-C

68069801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194004-T-G

http://identifiers.org/hco/8/GRCh38#68069804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11194007-C-A

68069804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194007-C-T

68069806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194009-T-C

68069806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194009-T-G

68069807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194010-G-A

68069807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194010-G-T

http://identifiers.org/hco/8/GRCh38#68069822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11194025-C-A

68069822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194025-C-G

68069822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194025-C-T

68069829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11194032-A-G

68069843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11194046-A-G

68069843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11194046-A-T

68069968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194143-G-A

68069968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194143-G-C

68069968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194143-G-T

68070009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194156-A-G

68070015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194162-A-G

68070140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194281-A-G

http://identifiers.org/hco/8/GRCh38#68070145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11194286-C-A

68070235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194388-G-A

http://identifiers.org/hco/8/GRCh38#68070237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11194390-A-C

68070237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194390-A-G

68070252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194426-A-G

68070324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194499-A-G

68070465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194618-C-G

68070776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194922-G-T

68070854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11195018-G-A

68070854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11195018-G-C

http://identifiers.org/hco/8/GRCh38#68070863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11195027-A-C

68070961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11195115-A-G

68071022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11195174-A-G

68071022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11195174-A-T

68071079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11195220-G-C

68071262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11195453-C-G

68071371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11195591-A-G

68071371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11195591-A-T

68071566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11195964-G-A

68071986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202268-A-G

68072287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202381-T-C

68072346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202430-T-G

http://identifiers.org/hco/8/GRCh38#68072388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11202468-C-A

http://identifiers.org/hco/8/GRCh38#68072399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11202478-C-A

68072399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202478-C-T

http://identifiers.org/hco/8/GRCh38#68072426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11202505-C-A

68072426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202505-C-G

68072426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202505-C-T

68072447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202526-G-A

68072447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202526-G-C

68072447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202526-G-T

http://identifiers.org/hco/8/GRCh38#68072486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11202553-C-A

68072486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202553-C-T

http://identifiers.org/hco/8/GRCh38#68072534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11202601-C-A

68072564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11202631-T-C

68072564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11202631-T-G

68072597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202664-G-A

68072597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202664-G-T

68072625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202690-A-G

68072646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202714-A-G

68072660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202728-G-A

68072660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202728-G-T

68072661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202729-T-A

68072666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202736-G-A

68072666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202736-G-T

68072667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202737-G-A

68072667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202737-G-T

68072695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202751-A-G

68072781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202827-G-A

68072781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202827-G-T

http://identifiers.org/hco/8/GRCh38#68072815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11202863-C-A

68072851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202940-G-C

68072851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11202940-G-T

68073024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11203099-G-A

68073232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11203295-A-G

68073315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11203369-G-A

68073329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11203381-T-A

68073355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11203406-T-C

68073380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11203431-T-C

68073781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11204881-C-T

68073916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11205015-A-G

68073916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11205015-A-T

68074442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11205214-A-G

68074714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11205397-C-G

68074857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11205539-C-G

68074897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11205578-A-G

68075431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11206045-A-G

68075545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11206140-A-G

68075553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11206148-C-T

68075618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11206220-C-G

68075715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11206315-A-G

68075731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11206334-C-T

68075753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11206354-G-A

68075878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11206463-A-G

68075963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11206519-C-T

68076126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11206670-A-T

68076499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11206755-T-A

68076501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11206756-A-T

68076522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11206777-G-T

68077337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11206925-A-G

http://identifiers.org/hco/8/GRCh38#68077374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11206962-C-A

http://identifiers.org/hco/8/GRCh38#68077376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11206964-C-A

68077376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11206964-C-T

68077593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11207175-G-A

68077823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11207394-G-C

68077953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11207510-T-C

68077985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11207543-G-C

68077985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11207543-G-T

68078116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11207594-G-A

68078248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11207689-C-G

68078257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11207698-G-A

68078282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11207720-C-T

68078290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11207728-G-A

68078307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11207744-A-G

68078500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11207901-T-C

68078673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11208056-C-T

68078674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11208057-G-A

68079431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11208593-A-G

68079547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11208708-A-G

68079568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11208717-T-C

68079622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11208782-G-A

68079753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11208910-T-C

68079863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11209021-G-A

68079888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11209046-A-T

http://identifiers.org/hco/8/GRCh38#68079906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11209064-C-A

68080161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11209924-G-A

68080185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11209943-A-G

68080277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210024-A-G

http://identifiers.org/hco/8/GRCh38#68080336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11210070-A-C

http://identifiers.org/hco/8/GRCh38#68080386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11210123-A-C

68080389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210126-A-G

http://identifiers.org/hco/8/GRCh38#68080652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11210382-C-A

68080817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11210531-A-G

68080852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210574-G-A

68080852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210574-G-C

http://identifiers.org/hco/8/GRCh38#68080979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11210663-C-A

68080979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210663-C-T

68081022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210708-G-A

68081067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210740-G-A

68081073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210746-T-C

68081517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210839-T-G

68081641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210961-C-T

68082175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11211621-G-A

68082175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11211621-G-C

68082175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11211621-G-T

68082178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11211624-G-T

http://identifiers.org/hco/8/GRCh38#68082179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11211625-C-A

http://identifiers.org/hco/8/GRCh38#68082204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11211650-C-A

68082214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211660-G-A

68082334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211783-A-G

68082335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211784-A-T

http://identifiers.org/hco/8/GRCh38#68082347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11211793-C-A

68082451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211898-T-C

http://identifiers.org/hco/8/GRCh38#68082475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11211921-C-A

68082479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211925-G-A

68082479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211925-G-T

68082495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211941-T-G

68082510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211954-A-G

68082510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211954-A-T

68082518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211961-G-T

68082652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11212086-G-A

68082652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11212086-G-T

68082671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11212104-G-A

68082718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11212164-A-G

68082719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11212165-G-A

68082719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11212165-G-T

68082758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11212202-C-G

http://identifiers.org/hco/8/GRCh38#68082777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11212224-C-A

http://identifiers.org/hco/8/GRCh38#68082859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11212312-A-C

68082973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11212600-A-T

http://identifiers.org/hco/8/GRCh38#68082974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11212601-C-A

http://identifiers.org/hco/8/GRCh38#68082980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11212607-A-C

68082980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11212607-A-G

68083011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11212653-A-G

68083012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11212654-T-G

68083032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11212675-T-C

68083118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11212755-G-A

68083118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11212755-G-T

68083131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11212768-A-G

http://identifiers.org/hco/8/GRCh38#68083138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11212775-A-C

68083138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11212775-A-G

68083138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11212775-A-T

68083144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11212781-A-G

68083144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11212781-A-T

http://identifiers.org/hco/8/GRCh38#68083169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11212805-C-A

68083169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11212805-C-T

68083335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11212968-G-A

http://identifiers.org/hco/8/GRCh38#68083386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11213019-A-C

68083386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 11213019-A-G

68083402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213035-T-C

http://identifiers.org/hco/8/GRCh38#68083494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11213110-A-C

68083494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213110-A-G

68083497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213113-G-A

68083497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213113-G-T

http://identifiers.org/hco/8/GRCh38#68083509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11213125-C-A

68083509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213125-C-T

68083514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213130-A-G

68083514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213130-A-T

68083519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213135-T-A

68083519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213135-T-C

68083519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213135-T-G

68083527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213143-G-A

68083527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213143-G-C

68083527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213143-G-T

http://identifiers.org/hco/8/GRCh38#68083533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11213149-A-C

68083533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213149-A-G

68083533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213149-A-T

68083534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213150-G-A

68083534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11213150-G-T

68083988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11214224-C-T

68084031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11214262-C-T

68084140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11214367-A-G

68084148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11214375-C-T

68084555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11214761-G-A

68084633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11214839-A-G

68084697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11214908-C-G

68084726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11214938-C-T

68084738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11214950-C-T

68084908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11215111-A-T

68085544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11217185-T-A

68085550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11217191-A-G

68085632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11217274-T-G

68085660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11217303-G-C

68085668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11217311-T-C

68085810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11217488-A-G

68085840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11217518-G-C

68085858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11217537-G-A

68085923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11217596-G-T

68086390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11218039-A-G

68086510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11218154-G-A

68086579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11218225-C-T

68087751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11220061-T-C

68087793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11220103-G-A

68087799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11220109-T-C

68087799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11220109-T-G

68087977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11220809-A-G

68087987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11220819-G-A

68087987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11220819-G-T

68088219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11221082-T-G

68088277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11221140-C-G

68088479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11221326-A-T

68088879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11221704-A-G

68088979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11221809-A-G

68089239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11222076-T-G

68089253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11222091-T-C

68089321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11222166-T-A

68089493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11222339-T-A

68089806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11222613-T-C

68089970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11222744-T-C

68090383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11223575-A-G

http://identifiers.org/hco/8/GRCh38#68090465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11223654-A-C

68090475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11223664-G-A

68090475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11223664-G-T

http://identifiers.org/hco/8/GRCh38#68090484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11223672-C-A

68090484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11223672-C-G

68090533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11223720-T-G

68090535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11223722-T-C

68090535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11223722-T-G

68090541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11223728-A-G

68090559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11223747-T-A

68090643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11223831-T-C

68090703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11223891-G-A

68090703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11223891-G-T

68090760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11223939-T-C

68090788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11223966-G-A

68090788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11223966-G-C

http://identifiers.org/hco/8/GRCh38#68090838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11224011-C-A

68090838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11224011-C-T

68090893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11224070-G-A

68090971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11224182-G-A

68091136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11224379-T-C

68091167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11224403-T-C

68091484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11224788-A-G

68091535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11224838-T-G

68091548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11224853-G-A

68091556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11224861-G-C

68091651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11224956-G-A

68091729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11225031-A-G

68091729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11225031-A-T

68091798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11225088-T-C

68092131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11225359-C-T

http://identifiers.org/hco/8/GRCh38#68092235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11225466-C-A

68092261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11225492-C-T

68092282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11225539-G-A

68092317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11225595-G-A

68092396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11225732-A-T

68092643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11225942-A-G

68092994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11226138-G-A

68092994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11226138-G-C

http://identifiers.org/hco/8/GRCh38#68093573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11226433-C-A

68093573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11226433-C-T

http://identifiers.org/hco/8/GRCh38#68093589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11226449-C-A

68093589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11226449-C-T

68093616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11226476-A-G

68093631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11226491-T-C

68093718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11226578-A-G

68093729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11226589-T-C

http://identifiers.org/hco/8/GRCh38#68093746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11226602-A-C

68093746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11226602-A-G

68093746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11226602-A-T

http://identifiers.org/hco/8/GRCh38#68093762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11226618-C-A

68093762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11226618-C-T

http://identifiers.org/hco/8/GRCh38#68093768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11226624-C-A

68093768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11226624-C-T

http://identifiers.org/hco/8/GRCh38#68093839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11226686-C-A

68093839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11226686-C-T

http://identifiers.org/hco/8/GRCh38#68093853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11226700-C-A

68093853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11226700-C-T

68094031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11227009-G-A

68094049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11227024-T-G

68094051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11227026-A-T

68094108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11227072-C-T

68094204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11227164-C-T

68094260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11227205-A-G

68094401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11227395-A-G

68094535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11227533-C-T

68094760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11227714-C-T

68094773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11227727-T-C

68094907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11227854-G-A

68094907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11227854-G-T

68094910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11227857-T-C

68094946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11227893-T-C

http://identifiers.org/hco/8/GRCh38#68094967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11227914-C-A

68095056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11228126-G-A

68095056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11228126-G-T

68095066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11228136-T-C

68095131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11228182-G-A

68095131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11228182-G-T

68095179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11228230-T-A

68095409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11228490-G-A

68095467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11228541-G-T

http://identifiers.org/hco/8/GRCh38#68095521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11228572-A-C

68095521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11228572-A-T

68095522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11228573-T-A

68095543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11228594-G-A

68095745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11228769-G-A

68095745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11228769-G-T

68095827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11228855-G-A

68095919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11228949-G-T

68096095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11229068-G-T

68096124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11229099-A-G

68096157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11229120-G-C

68096157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11229120-G-T

68096350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11229283-A-G

68096464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11229379-C-T

68096500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11229415-A-T

68096597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11229505-C-T

68096796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11229948-C-G

http://identifiers.org/hco/8/GRCh38#68096826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11229978-C-A

68096848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230000-G-A

68096871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230029-A-G

68096871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230029-A-T

http://identifiers.org/hco/8/GRCh38#68096948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11230259-C-A

68096961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230272-G-T

http://identifiers.org/hco/8/GRCh38#68096991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11230298-C-A

68096993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230300-G-C

68096998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230305-A-G

68097024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11230327-T-C

68097096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11230399-C-G

68097096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11230399-C-T

68097141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11230444-C-G

68097216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230519-G-T

68097245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230548-A-G

68097246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230549-G-A

http://identifiers.org/hco/8/GRCh38#68097296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11230585-C-A

68097302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230591-G-A

68097302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230591-G-T

68097308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230597-G-A

68097308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230597-G-T

http://identifiers.org/hco/8/GRCh38#68097319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11230607-C-A

68097319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230607-C-G

68097319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230607-C-T

68097327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230615-T-A

68097327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230615-T-C

68097336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230624-T-C

68097834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230794-G-A

68097856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230807-A-G

68097899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230828-A-G

68097935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11230851-C-T

http://identifiers.org/hco/8/GRCh38#68098164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11231054-C-A

68098244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11231136-T-C

68098281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11231169-T-G

68098532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11231379-T-C

68098562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11231409-A-G

68098790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11231612-G-T

68099363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11232245-T-C

http://identifiers.org/hco/8/GRCh38#68099414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11232296-C-A

68099734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11232516-G-C

68099822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11232604-G-A

68102416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11236754-T-C

68102444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11236782-T-C

http://identifiers.org/hco/8/GRCh38#68102460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11236798-A-C

68102527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11236853-G-A

68102598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11236922-A-G

68102648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11236971-C-T

68102689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11238164-C-G

http://identifiers.org/hco/8/GRCh38#68102726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11238197-A-C

68102873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11238311-C-T

68102894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11238332-A-G

68104992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11238541-C-T

68105008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11238557-T-G

68105060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11238605-A-G

68105064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11238609-G-A

68105109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11238651-A-G

68105110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11238652-T-C

68105110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11238652-T-G

68105111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11238653-T-C

68105172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11238719-C-T

68105176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11238723-G-A

68105176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11238723-G-T

68107107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11239119-T-G

68107139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11239148-G-C

68107345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11239350-T-G

68107524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11239522-C-G

68107796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11239787-T-C

68107826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11239816-A-G

68107935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11239917-G-C

68107974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11239946-A-G

68107974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11239946-A-T

http://identifiers.org/hco/8/GRCh38#68108001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11239975-C-A

68108003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11239977-T-C

68108003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11239977-T-G

http://identifiers.org/hco/8/GRCh38#68108016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11239990-C-A

68108016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11239990-C-T

68108028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11240002-T-C

68108028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11240002-T-G

68108036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11240010-A-G

68108036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11240010-A-T

http://identifiers.org/hco/8/GRCh38#68108040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11240014-A-C

68108040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11240014-A-G

68108210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11240178-T-C

68108216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11240184-T-C

http://identifiers.org/hco/8/GRCh38#68108400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11240354-C-A

http://identifiers.org/hco/8/GRCh38#68108428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11240382-C-A

68108428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11240382-C-T

68108448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11240402-T-C

68108463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11240417-T-C

http://identifiers.org/hco/8/GRCh38#68108466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11240420-C-A

68108466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11240420-C-T

68108692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11240629-A-G

68108737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11240675-C-T

68108782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11240720-G-A

68108782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11240720-G-T

68109435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11240827-G-T

68109447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11240839-C-T

68109526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 11240918-G-T

68109557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11240949-A-G

68109639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11241031-T-C

68109699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11241088-A-G

68109699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11241088-A-T

68109703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11241092-T-C

68109716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11241099-T-C

68109729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11241107-G-T

68109748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11241126-G-A

68109748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11241126-G-T

68109972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11241569-C-T

68110269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11241831-A-G

68111446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11246005-G-T

68111450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11246009-A-G

68111511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11246068-A-T

68111554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11246112-C-T

http://identifiers.org/hco/8/GRCh38#68111555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11246113-A-C

http://identifiers.org/hco/8/GRCh38#68111748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11246305-C-A

68111748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11246305-C-T

68112073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11246568-T-G

68112089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11246584-G-A

68112117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11246612-T-G

68112191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11246683-C-G

68112227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11246719-A-G

68112251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11246744-T-C

68112354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11246828-C-T

68112364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11246856-G-T

68112388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11246884-G-A

68112543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11247005-A-G

68112766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11249384-A-G

68112801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11249426-T-C

68112863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11249516-A-G

68112968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11249618-A-G

68113344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11249980-G-C

68113420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250055-G-A

68113543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250174-T-C

68113675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250305-A-T

68113987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250465-G-C

68114056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250513-T-A

68114185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250542-T-C

68114188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250545-A-G

68114192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250549-A-G

http://identifiers.org/hco/8/GRCh38#68114205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11250562-C-A

68114255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250604-A-T

68114260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250609-A-T

68114264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250613-A-G

http://identifiers.org/hco/8/GRCh38#68114280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11250629-C-A

68114384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250746-G-T

68114416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250778-G-A

68114434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250796-G-A

68114434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250796-G-T

68114467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250829-G-C

68114467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250829-G-T

68114515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250876-T-G

68114549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250904-G-A

68114577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250929-T-C

68114660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11250979-C-G

68114715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11251032-G-T

68114745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11251078-T-C

68115470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11251793-C-G

68115476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11251799-A-G

68115499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11251824-C-T

http://identifiers.org/hco/8/GRCh38#68115605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11251929-A-C

68115605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11251929-A-T

68115614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11251938-A-G

http://identifiers.org/hco/8/GRCh38#68115655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11251974-C-A

http://identifiers.org/hco/8/GRCh38#68115657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11251976-A-C

68115657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11251976-A-G

68115667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11251986-G-A

68115667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11251986-G-T

68115679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11251997-T-C

68115688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11252006-A-G

68115737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11252063-T-A

68115737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11252063-T-C

68115837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: synonymous variant
orthologous variants: 11252163-G-A

68115976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11252298-A-T

68116013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11252335-G-T

http://identifiers.org/hco/8/GRCh38#68116041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11252361-C-A

http://identifiers.org/hco/8/GRCh38#68116049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11252369-A-C

68116049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11252369-A-G

68116177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11252466-G-A

68116562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11252707-G-A

68116584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11252729-G-A

68116587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11252732-G-A

68116598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11252743-C-G

68116598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11252743-C-T

68116867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11252938-G-A

68117103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11253151-T-C

68117234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11253280-G-A

68117464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11253461-T-G

68117641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11253632-G-A

68117646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11253637-T-C

68117785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11253760-T-A

68117785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11253760-T-G

68117837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11253791-T-G

68117851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11253805-T-C

http://identifiers.org/hco/8/GRCh38#68118407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11254034-C-A

68118407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11254034-C-T

http://identifiers.org/hco/8/GRCh38#68118509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11254630-C-A

68118509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11254630-C-T

68118580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: synonymous variant
orthologous variants: 11254700-C-T

68118798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11254902-G-C

68118824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11254929-T-C

68118870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11254954-G-A

http://identifiers.org/hco/8/GRCh38#68118872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11254956-A-C

68118872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11254956-A-G

http://identifiers.org/hco/8/GRCh38#68118878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11254961-C-A

68118878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11254961-C-G

http://identifiers.org/hco/8/GRCh38#68118954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11255031-A-C

68118954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255031-A-G

68118954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255031-A-T

68118974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255052-G-A

68118974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255052-G-T

68118992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255080-T-C

68119049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255133-T-C

68119284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255248-G-T

68119345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255284-A-G

http://identifiers.org/hco/8/GRCh38#68119361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11255300-C-A

68119487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, missense_variant
orthologous variants: 11255409-T-A

68119523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255445-G-A

68119527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255449-A-G

68119539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255461-T-A

68119540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255462-T-C

68119558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255491-G-A

68119618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255542-A-T

http://identifiers.org/hco/8/GRCh38#68119625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11255549-C-A

68119625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255549-C-T

68119634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255558-T-A

68119634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255558-T-G

68119745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255657-T-G

68119820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255712-G-C

68119820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255712-G-T

68119825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255717-A-G

68120048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255953-A-G

http://identifiers.org/hco/8/GRCh38#68120071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11255976-C-A

68120071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255976-C-T

http://identifiers.org/hco/8/GRCh38#68120072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11255977-A-C

68120072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11255977-A-G

68120145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11256042-G-A

68120145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11256042-G-C

68120145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11256042-G-T

68120290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11256205-A-G

68120337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11256238-T-A

http://identifiers.org/hco/8/GRCh38#68120357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11256258-C-A

68120357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11256258-C-T

68120430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11256368-A-G

68120562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11256503-A-T

68120674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11256614-C-T

68120788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11256728-A-G

http://identifiers.org/hco/8/GRCh38#68120797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11256737-C-A

68120797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11256737-C-T

68120802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11256744-G-T

68120865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11256809-G-A

68120865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11256809-G-T

68120920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: splice acceptor variant
orthologous variants: 11256860-G-A

68120920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: splice acceptor variant
orthologous variants: 11256860-G-T

68120991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: synonymous variant
orthologous variants: 11256931-T-A

http://identifiers.org/hco/8/GRCh38#68121007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11256947-A-C

68121007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: missense variant
orthologous variants: 11256947-A-G

http://identifiers.org/hco/8/GRCh38#68121012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11256952-C-A

68121012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: synonymous variant
orthologous variants: 11256952-C-T

68121044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: missense variant
orthologous variants: 11256984-T-C

68121057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 11256997-T-C

68121332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11257254-A-G

68121350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11257272-A-G

68121351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11257273-T-C

68121794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11257530-A-G

http://identifiers.org/hco/8/GRCh38#68121849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11257587-C-A

68122314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11258000-G-A

68122545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11258230-T-C

68124218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11260308-C-G

68124229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11260319-A-G

68124389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11260479-G-C

68124618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11260740-C-T

http://identifiers.org/hco/8/GRCh38#68125171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11261228-A-C

68125339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11261399-G-A

68125507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11261551-G-A

68125892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11262484-C-T

68125901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11262493-T-A

68125927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11262514-T-G

68125928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11262515-A-G

68125962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11262541-A-G

68126023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11262597-G-A

68126068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11262645-C-T

68126115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11262693-G-C

http://identifiers.org/hco/8/GRCh38#68126333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11262893-C-A

68126664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11263214-A-G

68127147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11263588-G-A

68127301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11263658-T-C

68127329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11263688-T-C

http://identifiers.org/hco/8/GRCh38#68127417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: splice_region_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#11263776-C-A

68127502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11263854-G-A

68127502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11263854-G-T

68127515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11263873-T-C

68127565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11263928-G-A

http://identifiers.org/hco/8/GRCh38#68127653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11264033-C-A

68127658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11264053-C-T

68127912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11264372-G-A

http://identifiers.org/hco/8/GRCh38#68130436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11267029-A-C

68130694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11267362-A-T

68130725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11267385-G-T

68130763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11267421-G-A

http://identifiers.org/hco/8/GRCh38#68130891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11267544-A-C

68131102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11267727-C-T

68131185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11267786-G-A

68131309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11267905-G-A

68131320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11267916-G-T

68131322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11267918-T-G

68131396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11268002-A-G

68134060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 11270060-T-C

http://identifiers.org/hco/8/GRCh38#68134331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11270324-C-A

68134350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11270344-T-C

68134424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11270384-G-A

68134424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11270384-G-T

68134463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11270423-C-T

68134590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11270548-T-A

68134620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11270569-A-G

68134929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11270818-T-C

68134976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11270869-A-G

68135051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11270943-A-G

68135176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11271241-A-G

68135346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11271446-A-G

68135358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11271459-T-C

68135391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11271492-A-G

68135413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11271514-G-C

http://identifiers.org/hco/8/GRCh38#68135743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11271772-A-C

68135906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11272123-G-A

http://identifiers.org/hco/8/GRCh38#68135910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11272127-A-C

68135916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11272133-A-T

http://identifiers.org/hco/8/GRCh38#68135953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11272176-C-A

68135953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11272176-C-T

http://identifiers.org/hco/8/GRCh38#68136165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11272405-C-A

68136165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11272405-C-T

68136286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11272505-A-G

68137857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11273767-C-T

68137858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11273768-G-A

68137858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11273768-G-T

68137936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11273842-T-C

68137936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11273842-T-G

68138038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11273930-T-G

68138238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274129-G-C

68138375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274255-A-G

68138381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274257-T-C

68138383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274259-T-A

68138383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274259-T-C

http://identifiers.org/hco/8/GRCh38#68138407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11274283-C-A

68138407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 11274283-C-G

68138407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 11274283-C-T

68138595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274447-G-C

68138595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274447-G-T

68138607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274459-A-G

68138625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274461-A-G

68138632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274468-C-T

68138726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274567-C-T

68138727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274568-C-T

68138730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274571-A-G

68138757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274602-A-G

68139001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274860-C-T

68139109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11274970-T-G

68139210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11275054-G-A

68139289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11275125-G-A

68139322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11275160-C-G

68139322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11275160-C-T

68145315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11277383-A-G

68145340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11277403-A-T

68145467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11277517-A-G

68145668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11277714-A-G

68145807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11277844-C-T

http://identifiers.org/hco/8/GRCh38#68145846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11277883-C-A

68145846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11277883-C-T

68146026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278041-A-G

68146050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278068-A-G

68146062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278080-T-C

68146097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278600-G-A

68146097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278600-G-C

68146097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278600-G-T

68146105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278608-T-G

68146162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278689-G-A

68146162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278689-G-C

68146162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278689-G-T

http://identifiers.org/hco/8/GRCh38#68146163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11278690-C-A

68146164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278691-A-G

68146169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278696-C-T

68146179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278706-G-T

68146180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278707-A-G

68146187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278714-A-G

68146392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278917-A-T

68146403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278928-A-G

68146421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278947-G-A

68146421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278947-G-T

68146425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11278951-T-C

http://identifiers.org/hco/8/GRCh38#68146471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11279005-C-A

68146471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11279005-C-G

68146471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11279005-C-T

http://identifiers.org/hco/8/GRCh38#68146485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11279019-C-A

68146574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11279503-A-G

68147822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11280409-T-C

68148771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11280653-T-C

68148833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11280722-T-C

68148860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11280735-C-T

68148900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11280777-A-G

68148901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11280778-T-C

68148919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11280790-T-G

68149015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11280880-A-G

68149061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11280921-T-C

68149086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11280950-G-T

68149406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11281160-C-T

68149447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11281197-A-G

68149676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11281369-A-G

68149730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11281443-C-T

68149764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11281481-G-A

68149775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11281492-C-T

68149787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11281505-T-A

68149931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11281637-C-T

68150226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11281904-G-C

68150263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11281941-G-C

68153443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11282335-T-G

68153483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11282375-A-T

68153648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11282599-T-C

68153692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11282647-G-A

68153745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11282699-C-G

68153796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11282756-C-G

http://identifiers.org/hco/8/GRCh38#68153802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11282762-A-C

68153812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11282772-G-A

68154000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11282945-A-G

68154291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11283174-C-T

http://identifiers.org/hco/8/GRCh38#68154365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11283273-A-C

68154468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11283387-T-A

68155707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11284031-G-C

68155741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11284063-C-T

68155923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11284281-T-A

68157036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11301642-C-T

68157037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11301643-G-A

http://identifiers.org/hco/8/GRCh38#68157263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11301850-A-C

68157263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11301850-A-G

68157263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11301850-A-T

68157392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11301976-T-C

68157763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302330-T-C

68157807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302374-C-T

68157868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302430-G-T

68168309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11311724-A-G

68168316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11311731-T-C

68168347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11311753-A-G

68168349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11311755-A-G

68168439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11311812-G-C

68168806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312155-C-T

68168845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312194-T-C

68168878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312223-G-C

68168878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312223-G-T

68168943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312263-C-T

68169025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312347-G-A

68169138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312445-G-A

68169171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312486-C-T

68169254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312557-G-A

68169290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312583-G-C

http://identifiers.org/hco/8/GRCh38#68169848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11312998-C-A

68169899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11313117-A-G

68170558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11313896-G-A

68170905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11314295-A-G

68171020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11314390-G-C

68171232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11314610-C-T

68171295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11314914-T-A

68171295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11314914-T-C

68171364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11314977-A-T

68171647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11315269-C-G

68171647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11315269-C-T

68171791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11315437-T-A

68172227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11315851-A-G

68172297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11315923-T-C

68172298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11315924-G-C

68172388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11316009-G-A

68172472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11316090-T-C

68172763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11316379-G-C

68172763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11316379-G-T

68172784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11316398-G-T

http://identifiers.org/hco/8/GRCh38#68173023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11316631-C-A

http://identifiers.org/hco/8/GRCh38#68173391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11317004-C-A

68173391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11317004-C-T

68173430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11317042-T-C

68173509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11317120-A-G

68173578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11317182-T-C

http://identifiers.org/hco/8/GRCh38#68173622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11317226-A-C

68173714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11317318-T-C

68173972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11317640-G-T

68174034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11317693-G-A

68174157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11317830-A-G

68174273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11317905-G-C

68174401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318012-C-T

68174466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318056-C-G

68174579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318168-T-A

68174579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318168-T-C

http://identifiers.org/hco/8/GRCh38#68174583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11318172-C-A

68174583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318172-C-T

68174673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318263-A-G

68174723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318305-G-T

68175572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318484-A-T

68175721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318632-G-A

68175773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318675-C-T

68175832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318731-A-G

68175876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318775-A-T

68175923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318824-G-T

68176197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319257-A-G

68176273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319325-T-C

68176492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319524-C-T

http://identifiers.org/hco/8/GRCh38#68176705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11319704-C-A

68176813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11319795-T-G

68176868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11319847-G-C

68176886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11319865-C-T

http://identifiers.org/hco/8/GRCh38#68176888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11319867-C-A

68176953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11319932-T-C

68176993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11319964-T-A

68177203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11320126-G-T

68180591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11321959-G-A

68180725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11322085-A-T

68180782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11322117-G-C

68180853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11322160-G-T

68180867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11322174-A-G

68181287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11322562-C-T

68184576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11322833-C-G

68184873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323133-T-C

68184903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323162-G-C

68185042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323298-C-T

68185046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323302-C-T

68185096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323350-T-A

68185117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323372-G-A

68185124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323379-T-C

68185179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323425-G-A

68185213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323448-G-A

68185332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323575-C-G

68185631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323853-T-C

68185978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11324218-A-T

68186191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11324422-T-C

68186912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11325019-C-T

http://identifiers.org/hco/8/GRCh38#68187246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11325320-C-A

68187474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11325736-A-G

68187872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326058-G-A

http://identifiers.org/hco/8/GRCh38#68187903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11326088-A-C

68187915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326099-G-C

68187999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326194-T-C

http://identifiers.org/hco/8/GRCh38#68188053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11326238-C-A

68188105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326291-G-T

68188145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326319-C-G

68188171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326345-G-A

68188171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326345-G-C

http://identifiers.org/hco/8/GRCh38#68188205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11326381-A-C

68188205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326381-A-G

68188256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326430-A-G

http://identifiers.org/hco/8/GRCh38#68188407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11326569-C-A

68189115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11334791-A-T

68189262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11334931-C-T

68189280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11334953-T-C

68189288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11334954-G-A

68189288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11334954-G-C

68189465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11335119-A-G

68189475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11335129-G-A

68189742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11335343-A-T

68189853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11335443-A-G

68189980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11335564-G-A

68191558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11335738-A-G

68191574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11335752-G-T

68191627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11335806-G-T

68191658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11335837-A-T

68191775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11335956-C-T

68192212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336062-T-C

68192239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336088-T-C

http://identifiers.org/hco/8/GRCh38#68192316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11336175-C-A

68192316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336175-C-T

68192320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336179-A-G

68192529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 11336387-T-C

68192640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336484-G-A

68192640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336484-G-T

http://identifiers.org/hco/8/GRCh38#68192712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11336553-A-C

68192712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336553-A-G

68192712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336553-A-T

68192713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336554-T-A

68192713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336554-T-G

http://identifiers.org/hco/8/GRCh38#68192723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11336564-C-A

http://identifiers.org/hco/8/GRCh38#68192757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11336598-C-A

68192757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336598-C-T

http://identifiers.org/hco/8/GRCh38#68192772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11336613-A-C

68192772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336613-A-G

http://identifiers.org/hco/8/GRCh38#68192780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11336621-A-C

68192780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336621-A-G

68192885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336730-A-T

68192970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336816-A-G

68193021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336875-G-A

68193078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336889-C-T

http://identifiers.org/hco/8/GRCh38#68193185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11336951-A-C

68193185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11336951-A-G

68193287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11337050-C-G

68193393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11337070-A-G

68193442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11337088-G-C

68193624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11337268-T-C

68193700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11337327-G-A

68193780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11337404-A-G

68193899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11337485-C-T

68194274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11337719-C-T

68194320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11337758-T-C

68195117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338160-G-A

68195225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338263-T-A

68195239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338270-C-T

68195251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338282-A-G

68195287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338322-A-G

68195288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338323-T-A

68195407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338425-T-C

68195566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338585-C-T

68195640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338658-C-T

68195667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338685-G-A

68195667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338685-G-T

68195758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338766-T-A

68195764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338772-T-A

68195773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338783-T-C

68195830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338824-G-C

68195838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338832-T-C

68195930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338892-A-T

68196006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338937-T-G

68196081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11339010-T-C

68196149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11339063-C-T

68196298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11339131-T-A

68196307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11339140-G-A

68196307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11339140-G-T

http://identifiers.org/hco/8/GRCh38#68198033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11339655-C-A

68198033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11339655-C-G

68198033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11339655-C-T

68198213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11339808-C-T

68198281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11339864-A-G

68198336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11339922-C-G

68198336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11339922-C-T

68198597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340199-T-C

68198951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340512-G-A

68199021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340576-G-A

68199030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340585-T-A

68199079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340632-T-C

68199252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340771-A-G

68199326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340867-G-A

http://identifiers.org/hco/8/GRCh38#68199469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11340986-C-A

68199996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11341477-T-C

68199996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11341477-T-G

http://identifiers.org/hco/8/GRCh38#68200158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11341633-A-C

68203124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11342461-T-C

68203391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11342718-A-G

68203606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11342903-G-A

http://identifiers.org/hco/8/GRCh38#68203738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11343017-C-A

68203846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11343122-G-A

68203979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11343244-T-C

68204017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11343282-C-G

68204167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11343413-T-C

68204321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11343566-C-T

68204343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11343587-C-T

68204470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11343875-G-A

68204470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11343875-G-C

68204483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11343888-C-T

68204485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11343890-C-T

68204628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11344026-A-G

68204644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11344042-C-T

68205312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11344262-C-T

68205437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11344371-A-G

68205441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11344375-A-G

68205474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11344409-C-T

68205534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11344468-T-A

68205569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11344505-A-G

68205738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11344677-G-A

68205738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11344677-G-C

68205890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11344825-C-T

68206001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11344936-C-T

68206101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11345032-G-C

68206123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11345054-A-T

68206131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11345062-T-C

68206198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11345126-G-A

68206278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11345206-A-G

68206324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11345244-T-A

68206324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11345244-T-C

68206648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11345624-C-T

68206803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11345767-G-C

68207277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346099-G-A

68207277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346099-G-T

68207343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346163-C-T

68207368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346188-C-T

68207483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346297-G-A

68207522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346336-A-T

68207755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11347220-G-A

68207760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11347225-A-G

68207834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11347298-C-T

68208180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11347630-G-C

68208236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11347686-G-A

68208456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11347859-A-T

68208699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11348614-T-G

68208776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11348671-A-G

68209304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11348866-A-G

68210078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11349198-G-C

68210229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11349339-A-T

68210270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11349373-C-T

68210331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11349432-C-T

68210333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11349434-C-G

68210333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11349434-C-T

68210359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11349460-G-A

68210473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11349616-G-A

68210493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11349632-A-G

http://identifiers.org/hco/8/GRCh38#68212800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11350567-A-C

68212869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11350619-T-C

68213219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11350964-C-T

68213296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11351053-T-A

68213353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11351110-T-G

68213396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11351152-G-A

68213592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11351624-G-A

68213809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11351819-C-G

68213809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11351819-C-T

68213848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11351851-G-A

68213913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11351918-C-T

68214410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11352158-G-A

68214427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11352175-G-A

68214428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11352176-A-G

68214439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11352195-C-G

68214439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11352195-C-T

68214497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11352253-A-T

68214728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11352455-G-A

68214895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11352643-T-C

68215331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11353115-A-G

68215331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11353115-A-T

68215860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11353321-A-G

68215881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11353341-G-A

68217546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355214-G-A

68217546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355214-G-C

68217546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355214-G-T

68217604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355269-C-T

68217608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11355273-G-T

68217644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11355309-G-A

http://identifiers.org/hco/8/GRCh38#68217725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11355390-C-A

68217726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11355391-T-A

68217794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355450-G-A

68217794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355450-G-T

68217820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355453-G-T

68217833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355466-G-A

68217833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355466-G-T

68217942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355569-G-A

68217968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355592-T-A

68217968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355592-T-G

68217973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355597-T-G

68218159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355774-C-T

http://identifiers.org/hco/8/GRCh38#68218307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11355916-A-C

68219170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11356716-C-T

68219188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11356732-C-T

68219548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11357079-G-A

68219821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11357358-A-T

68220331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11357957-T-G

68220351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11357977-G-A

68220351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11357977-G-T

68220433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11358061-G-T

http://identifiers.org/hco/8/GRCh38#68223496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11358682-C-A

68223525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11358709-T-A

68223536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11358719-T-C

http://identifiers.org/hco/8/GRCh38#68223744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11358955-C-A

68223797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11359015-C-T

68223886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11359109-T-C

68224443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11359384-A-G

http://identifiers.org/hco/8/GRCh38#68224523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11359452-C-A

68224523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11359452-C-T

68224633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 11359551-G-A

68224652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11359568-T-G

68224673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11359585-T-C

68224686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11359598-T-C

http://identifiers.org/hco/8/GRCh38#68224903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#11359797-A-C

68225307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11360223-C-T

68225442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11360332-G-C

68225524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11360413-A-T

68225798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11360672-A-T

68225812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11360694-C-G

68225812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11360694-C-T

68225813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11360727-G-A

68225813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11360727-G-C

68225844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11360757-G-A

68225930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11360843-C-T

68225949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11360863-G-A

68225959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11360873-G-A

68226105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11361017-G-T

68226235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11361128-A-G

68226487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11361562-G-A

68226540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11361616-T-A

68226655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11361742-C-T

68228042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11362149-G-A

68228265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22950
most severe consequence: intron variant
orthologous variants: 11362288-T-G