46476974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3 prime UTR variant
orthologous variants: 77530083-C-T

46477003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3 prime UTR variant
orthologous variants: 77530053-G-A

46477003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3 prime UTR variant
orthologous variants: 77530053-G-T

46477007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3 prime UTR variant
orthologous variants: 77530033-A-G

46477034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3 prime UTR variant
orthologous variants: 77530006-T-C

http://identifiers.org/hco/18/GRCh38#46477352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77529669-C-A

46477354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77529667-G-T

http://identifiers.org/hco/18/GRCh38#46477359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77529647-C-A

46477380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77529628-G-T

http://identifiers.org/hco/18/GRCh38#46477388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77529619-C-A

46477388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77529619-C-T

46477500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, missense_variant
orthologous variants: 77529535-G-A

46477500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, missense_variant
orthologous variants: 77529535-G-C

46477500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, missense_variant
orthologous variants: 77529535-G-T

46477749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77529286-T-A

46477749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77529286-T-C

46477791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77529244-G-A

46478157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77528981-G-A

46478202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77528935-T-C

http://identifiers.org/hco/18/GRCh38#46478340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77528880-C-A

46478340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77528880-C-T

46478348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77528872-C-T

46478349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77528871-G-A

46480054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77520877-G-A

46480425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77520504-C-T

46480572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77520355-A-T

46480627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77520332-C-G

46480647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77520308-G-A

46480845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77520109-T-C

46480884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77520064-T-C

http://identifiers.org/hco/18/GRCh38#46483509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77518974-C-A

46483509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77518974-C-G

46483509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77518974-C-T

http://identifiers.org/hco/18/GRCh38#46483563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77518943-C-A

46483563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77518943-C-T

46483596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77518910-T-A

46483798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77518709-T-C

46483855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77518672-G-A

46483855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77518672-G-T

46483873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77518654-A-G

46484211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77518345-C-G

46484346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77518217-A-G

46484390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77518173-G-T

46484419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77518151-C-T

46484450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77518115-T-G

46484469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77518093-T-C

46484603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77517992-T-C

46484603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77517992-T-G

46484650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77517949-A-T

46484673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77517930-C-T

46484896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77517804-T-C

46484951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77517777-G-A

46484951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77517777-G-C

46484951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77517777-G-T

http://identifiers.org/hco/18/GRCh38#46484961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77517767-C-A

46484961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77517767-C-T

http://identifiers.org/hco/18/GRCh38#46484984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77517750-C-A

46484984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77517750-C-T

46484985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77517749-C-T

46485028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77517709-G-A

46485275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77517476-G-A

46485275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77517476-G-T

46485536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77517200-C-T

46485622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77517120-A-G

http://identifiers.org/hco/18/GRCh38#46485772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77516974-C-A

46485853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77516896-C-T

46485929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77516833-T-A

46485929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 77516833-T-C

46487449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77515598-G-A

46487918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77515230-A-T

46488076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77515085-G-T

46488083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77515078-T-G

46488102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77515061-T-A

46488312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77514262-G-A

46488340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77514234-C-T

46488379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77514177-C-T

46488484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77514073-C-G

46488531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77514022-T-C

http://identifiers.org/hco/18/GRCh38#46488587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77513979-C-A

46488663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513905-C-T

46488687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513728-G-A

46488802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513626-G-A

46488839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513595-G-A

46488839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513595-G-T

http://identifiers.org/hco/18/GRCh38#46488872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77513532-C-A

46488884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513520-A-T

46488904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513500-G-T

46488908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513492-G-A

46488908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513492-G-T

46488920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513480-T-C

46488931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513469-T-C

http://identifiers.org/hco/18/GRCh38#46488945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77513459-C-A

46488945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513459-C-G

46488946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513458-C-G

46488966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513453-A-G

46488966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513453-A-T

46489111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: synonymous variant
orthologous variants: 77513308-G-A

46489111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: synonymous variant
orthologous variants: 77513308-G-C

46489181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513246-G-A

46489181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513246-G-T

46489185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513242-T-C

46489186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513241-C-T

46489440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77513016-T-C

http://identifiers.org/hco/18/GRCh38#46489501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77512953-C-A

http://identifiers.org/hco/18/GRCh38#46489506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77512948-A-C

46489758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77512721-C-T

46489879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77512639-A-G

46489937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77512574-G-C

46490223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77512312-G-A

46490223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77512312-G-C

46490231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77512311-C-T

46490236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77512306-G-A

46490866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77510263-A-G

46490885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77510245-C-T

http://identifiers.org/hco/18/GRCh38#46491958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77509962-A-C

46491991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77509924-T-G

46493094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77508607-T-A

46493529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77508216-C-T

46493800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77507954-G-A

46493974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77507847-G-T

46494064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77507759-T-C

46494106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77507405-G-T

46494582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77506964-A-G

46495347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77506626-A-G

46496100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77506134-T-A

46496129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77506102-A-T

46496290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77506012-G-A

46496290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77506012-G-T

46496316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77505986-A-G

46496335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77505954-A-G

46497385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, undefined
orthologous variants: 77505331-G-A

46498011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77504328-C-T

46504564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77503040-T-C

46504582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77503018-A-G

46504601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77503001-T-C

46504604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77502998-T-C

46504863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77502766-G-C

46505024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77502608-A-G

http://identifiers.org/hco/18/GRCh38#46505069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77502568-A-C

46505660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77502107-C-T

46505750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77502025-A-G

46505750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77502025-A-T

46505772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77502009-G-A

46505772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77502009-G-T

46505779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77502002-G-A

46505795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77501984-T-C

http://identifiers.org/hco/18/GRCh38#46505806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77501975-C-A

46505806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77501975-C-T

46505846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77501935-T-C

http://identifiers.org/hco/18/GRCh38#46505959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77501822-C-A

46506011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77501770-T-C

46506051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77501730-G-C

http://identifiers.org/hco/18/GRCh38#46506107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77501676-C-A

http://identifiers.org/hco/18/GRCh38#46506125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77501648-A-C

46506125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77501648-A-G

46506137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77501636-T-A

46506137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77501636-T-C

46506167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77501573-G-A

46506167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77501573-G-T

46506327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77501214-C-T

46506328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77501213-G-A

46506330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77501211-G-A

46506333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77501208-A-G

46506563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77500939-A-G

46506585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77500913-G-A

46506585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77500913-G-C

46506682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77500816-T-C

46506716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77500780-A-G

46506792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77500708-C-T

46507194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77500277-G-A

46507199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77500272-T-G

46507439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77500095-T-A

46507439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77500095-T-C

46507721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77499828-G-A

46507721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77499828-G-C

46507721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77499828-G-T

http://identifiers.org/hco/18/GRCh38#46507729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77499820-C-A

46507729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77499820-C-T

http://identifiers.org/hco/18/GRCh38#46507758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77499789-C-A

http://identifiers.org/hco/18/GRCh38#46508022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77499614-A-C

46508359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77499318-A-G

46508359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77499318-A-T

http://identifiers.org/hco/18/GRCh38#46508535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77499163-C-A

46508535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77499163-C-G

46508621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77499111-T-C

46508928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77498940-T-C

46508928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77498940-T-G

46509054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77498825-G-A

46509074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77498806-G-A

46509433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77498491-T-C

46509433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77498491-T-G

http://identifiers.org/hco/18/GRCh38#46509439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77498485-A-C

46509439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77498485-A-G

46509439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77498485-A-T

http://identifiers.org/hco/18/GRCh38#46509510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77498435-C-A

46509656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77498348-G-T

46509681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77498330-G-A

46509681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77498330-G-T

46509682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77498329-G-T

46509687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77498324-A-G

46509688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77498323-G-T

46509837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77498182-A-G

46509837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77498182-A-T

46509874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77498159-T-A

46509874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77498159-T-G

http://identifiers.org/hco/18/GRCh38#46509884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77498149-C-A

46509884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77498149-C-T

http://identifiers.org/hco/18/GRCh38#46510029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77498036-C-A

46510029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77498036-C-T

46510288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77497816-A-G

46510511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77497634-A-G

46510526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77497619-A-G

46510526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77497619-A-T

46510588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77497560-G-T

46510748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77497406-G-A

46517991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77496652-G-T

46518009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77496635-G-T

46518085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77496566-G-A

46518085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77496566-G-T

46518086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77496565-T-G

http://identifiers.org/hco/18/GRCh38#46518089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77496562-A-C

46518146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77496506-C-G

46518146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77496506-C-T

46518264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77496388-G-A

46518264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77496388-G-T

46518277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77496376-G-A

46518330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77496325-C-T

http://identifiers.org/hco/18/GRCh38#46518351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77496303-C-A

46518351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77496303-C-G

46518351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77496303-C-T

46518362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77496292-G-A

46518362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77496292-G-C

46518362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77496292-G-T

46518379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77496275-T-C

http://identifiers.org/hco/18/GRCh38#46518401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77496255-C-A

46518478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77496206-C-T

46518574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77496161-G-A

46518652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77496085-G-A

46518652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77496085-G-C

46518795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77495808-T-A

46518795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77495808-T-C

46518795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77495808-T-G

http://identifiers.org/hco/18/GRCh38#46518820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77495785-C-A

46518820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77495785-C-T

46518936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495660-G-A

46518936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495660-G-T

http://identifiers.org/hco/18/GRCh38#46518978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77495637-C-A

46518978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495637-C-G

46518982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495633-A-G

http://identifiers.org/hco/18/GRCh38#46519004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77495611-C-A

46519021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495591-G-A

46519036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495576-C-T

46519037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495575-C-T

46519079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495536-T-C

46519110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77495513-A-G

46519124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77495502-G-C

46519124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77495502-G-T

46519155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77495471-T-C

46519156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77495470-T-A

http://identifiers.org/hco/18/GRCh38#46519180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77495446-C-A

46519209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77495419-G-A

46519209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77495419-G-T

46519214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77495414-A-G

46519215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77495413-G-T

46519349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495339-A-G

46519382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495302-A-G

46519405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495277-G-A

46519508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495185-T-C

46519607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495144-A-T

46519653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495100-A-G

46519687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495067-C-G

46519687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495067-C-T

46519732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77495031-T-A

46519818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77494945-A-T

46519865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77494907-C-T

46519895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77494880-A-G

46519954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77494821-G-A

46520153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77494646-T-A

46520157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77494642-G-T

http://identifiers.org/hco/18/GRCh38#46520386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77494470-C-A

http://identifiers.org/hco/18/GRCh38#46520391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77494464-C-A

46520391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77494464-C-T

46520474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77494389-A-G

46520488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77494375-G-A

46520488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77494375-G-C

http://identifiers.org/hco/18/GRCh38#46520543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77494324-C-A

46520543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77494324-C-T

46520594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77494287-T-C

http://identifiers.org/hco/18/GRCh38#46520727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77494025-A-C

46520727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77494025-A-G

46520779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77493973-G-A

46520779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77493973-G-T

46520849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77493904-C-G

46520849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77493904-C-T

46520910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77493843-C-G

http://identifiers.org/hco/18/GRCh38#46521015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77493742-C-A

46521015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77493742-C-G

46521015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77493742-C-T

46521122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77493671-G-A

46521140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77493653-A-G

46521140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77493653-A-T

46521285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77493508-A-G

http://identifiers.org/hco/18/GRCh38#46521372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77493404-C-A

46521381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77493395-T-C

46521607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77493175-G-A

46521655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77493135-G-T

http://identifiers.org/hco/18/GRCh38#46521695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77493096-A-C

46521717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77493074-G-A

46521717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77493074-G-T

46521746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77493045-C-G

46522045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77492760-T-G

http://identifiers.org/hco/18/GRCh38#46522046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77492759-C-A

46522046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77492759-C-G

46522046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77492759-C-T

46522069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77492731-G-T

http://identifiers.org/hco/18/GRCh38#46522114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77492688-A-C

46522114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77492688-A-G

46522132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77492670-C-T

46522219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77492583-T-C

46522273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77492529-T-A

46522345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77492457-C-G

46522345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77492457-C-T

46522530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77492260-A-G

46523080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491952-T-C

46523227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491876-A-G

46523274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491853-C-T

46523318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491823-C-G

46523525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491627-A-T

46523585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491569-C-T

46523586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491568-G-A

46523628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491528-T-C

46523883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491270-T-C

46523928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491238-A-G

http://identifiers.org/hco/18/GRCh38#46523979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77491186-A-C

46524069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491104-G-A

46524138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77491047-C-T

46524241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77490855-T-C

46524354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77490775-T-C

46524374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77490753-A-G

http://identifiers.org/hco/18/GRCh38#46524400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77490726-C-A

46524400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77490726-C-G

46524417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77490709-C-T

http://identifiers.org/hco/18/GRCh38#46524435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77490691-C-A

46524435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77490691-C-G

http://identifiers.org/hco/18/GRCh38#46524519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77490607-A-C

46524519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77490607-A-G

46524790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77490299-T-G

46524921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77490168-G-A

46524921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77490168-G-C

46524921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77490168-G-T

http://identifiers.org/hco/18/GRCh38#46525050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/18/GRCm39#77490063-C-A

46525050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77490063-C-T

46526257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489687-G-C

46526387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489575-G-A

46526492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489465-C-T

46526684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489281-T-G

46526850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489170-T-C

46526882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489138-T-C

46526984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77489032-A-T

46527041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488978-A-G

46527048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488971-G-A

46527048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488971-G-T

46527172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488695-T-G

46527355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488508-G-A

46527355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488508-G-C

46527387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488476-G-A

46527473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488400-C-T

46527762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488137-G-A

46527762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77488137-G-C

46527800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487973-A-G

46527800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487973-A-T

46527833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487941-G-A

46527833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487941-G-C

46527894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487885-G-A

46527945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487842-T-A

http://identifiers.org/hco/18/GRCh38#46528032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77487764-A-C

46528033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487763-G-A

46528105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487691-T-A

46528159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487663-T-C

http://identifiers.org/hco/18/GRCh38#46528176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77487647-C-A

46528248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487587-T-C

46528493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487384-G-C

46528695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487205-G-C

46528836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487080-G-A

46528870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77487046-A-G

http://identifiers.org/hco/18/GRCh38#46529039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77486908-C-A

46529111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77486857-G-A

46529111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77486857-G-C

46529111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77486857-G-T

46529347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486651-G-A

46529347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486651-G-T

46529377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486621-G-A

46529383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486615-G-A

46529383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486615-G-C

46529411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486588-G-T

46529449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486554-T-C

46529479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486523-G-A

46529479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486523-G-T

46529649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486369-A-G

46529662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486368-G-T

46529679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486351-A-T

46529876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486174-A-G

46529885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486165-C-T

46529886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77486164-G-A

46530068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485988-A-T

46530103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485949-C-T

46530499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485759-C-G

46530499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485759-C-T

46530613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485650-A-G

46530615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485648-G-C

46530615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485648-G-T

46530645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485618-T-C

46530838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485463-C-T

46530931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485362-C-T

46530933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485360-T-C

46530989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485306-G-A

46530999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485296-C-T

46531045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485252-C-T

46531101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485213-C-T

http://identifiers.org/hco/18/GRCh38#46531190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77485132-C-A

46531192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485130-G-A

46531192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77485130-G-T

46531337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77484995-T-C

46532012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77484365-T-C

46532251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77484116-T-C

http://identifiers.org/hco/18/GRCh38#46532294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77484067-C-A

46532375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77484019-G-A

46532386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77484011-A-T

46532610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77483798-G-A

46532689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77483699-G-A

http://identifiers.org/hco/18/GRCh38#46533026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77483359-C-A

46533026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77483359-C-T

46533097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77483296-G-T

46533108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77483285-G-A

46533108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77483285-G-C

46533108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77483285-G-T

46533227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77483113-G-C

46533330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77483010-G-A

46533330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77483010-G-T

46533355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482985-C-T

46533382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482958-G-T

46533401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482936-T-C

46533419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482918-A-G

http://identifiers.org/hco/18/GRCh38#46533544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77482802-A-C

46533602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482742-A-T

46533605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482739-G-A

46533605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482739-G-T

46533646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482707-G-A

46533646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482707-G-T

46533961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482494-C-T

46534043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482397-G-A

46534043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482397-G-T

46534131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482321-C-T

46534170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482294-A-T

46534246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482261-T-C

46534269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482247-A-G

46534309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482211-G-T

46534320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482200-C-G

46534320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482200-C-T

46534509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482026-T-C

http://identifiers.org/hco/18/GRCh38#46534523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77482012-C-A

46534523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77482012-C-T

46534574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77481957-T-C

http://identifiers.org/hco/18/GRCh38#46534617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77481910-C-A

46534617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77481910-C-T

46534782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77481757-C-T

46534865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77481672-T-C

46534890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77481648-T-C

46534895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77481643-G-A

46534895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77481643-G-C

46534895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77481643-G-T

46535911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77480763-T-C

46536114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77478030-T-C

46536185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77477959-C-T

46536272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77477878-G-A

46536314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77477844-T-A

46536314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77477844-T-C

46536314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77477844-T-G

46536316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77477842-G-A

46536349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77477803-C-G

46536404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77477769-G-C

46536472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77477705-T-A

46536559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77477622-G-A

46536800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77477412-C-G

46536871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77477344-C-T

46536891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77477323-C-T

46536989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77477251-T-A

46537322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77476934-T-C

46537757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77476521-A-G

http://identifiers.org/hco/18/GRCh38#46538083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77476253-C-A

46538083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77476253-C-G

46538101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77476247-C-T

46538244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77476124-A-G

46538247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77476121-G-A

46538280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77476088-G-A

46538289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77476079-C-G

46538289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77476079-C-T

46538390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77475977-A-G

http://identifiers.org/hco/18/GRCh38#46538404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77475963-C-A

46538404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77475963-C-G

46538404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77475963-C-T

46538467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77475947-G-A

46538467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77475947-G-C

46538467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77475947-G-T

http://identifiers.org/hco/18/GRCh38#46538539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77475914-A-C

http://identifiers.org/hco/18/GRCh38#46538565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77475888-A-C

46538570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77475883-G-A

http://identifiers.org/hco/18/GRCh38#46538905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77475590-C-A

46539103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77475318-G-A

46539114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77475307-T-C

46539147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77475283-T-C

46539851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77474545-C-G

46540004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77474388-A-G

http://identifiers.org/hco/18/GRCh38#46540079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77474331-C-A

46540079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77474331-C-T

46540470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77473939-C-T

46540494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77473919-G-T

http://identifiers.org/hco/18/GRCh38#46540538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77473887-C-A

46540679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77473749-G-T

46540834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77473609-C-T

http://identifiers.org/hco/18/GRCh38#46541120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77473348-A-C

46541120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77473348-A-G

46541120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77473348-A-T

46541123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77473345-T-G

46541582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77473035-A-G

46541609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77473008-G-T

46541619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77472935-C-T

46541621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77472933-C-G

http://identifiers.org/hco/18/GRCh38#46541680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77472869-C-A

46541690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77472859-A-G

46541699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77472850-G-A

46541720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77472829-G-T

46541944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77472612-G-A

46541978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77472573-G-C

46541978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77472573-G-T

46542000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77472551-G-A

46542000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77472551-G-T

46542021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77472530-T-G

http://identifiers.org/hco/18/GRCh38#46542053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77472493-A-C

46542053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77472493-A-G

46542053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77472493-A-T

46542306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77472229-C-G

46542306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77472229-C-T

46542510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77471720-C-T

46542517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77471713-G-A

46542679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77471594-C-T

46542703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77471570-G-T

http://identifiers.org/hco/18/GRCh38#46542917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77471356-C-A

46542917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77471356-C-T

http://identifiers.org/hco/18/GRCh38#46542919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77471354-C-A

46542919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77471354-C-T

http://identifiers.org/hco/18/GRCh38#46543692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77470718-C-A

46543930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77470490-C-T

46544071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77470361-T-C

46544543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77470002-G-A

http://identifiers.org/hco/18/GRCh38#46544756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77469802-C-A

46544756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469802-C-T

46544788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469785-G-A

46544788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469785-G-C

46544866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469724-G-A

46544939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469659-G-A

46544960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469631-C-T

http://identifiers.org/hco/18/GRCh38#46544984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77469607-A-C

46544984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469607-A-G

46544984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469607-A-T

46544993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469592-A-T

46545022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469571-T-A

46545022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469571-T-C

46545096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469492-G-A

46545239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469381-C-G

http://identifiers.org/hco/18/GRCh38#46545463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77469194-C-A

46545470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469187-T-A

46545470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469187-T-C

46545516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469155-G-T

http://identifiers.org/hco/18/GRCh38#46545531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77469140-C-A

46545531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469140-C-G

46545531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469140-C-T

http://identifiers.org/hco/18/GRCh38#46545567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77469107-C-A

http://identifiers.org/hco/18/GRCh38#46545627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77469052-C-A

46545627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77469052-C-T

46546035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77468978-T-C

46546103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77468903-C-G

46546140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77468866-G-A

46546807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77468335-G-A

46546807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77468335-G-T

46546859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77468286-G-A

46546865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77468280-G-A

46546865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77468280-G-C

46546879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77468266-C-T

46546942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77468203-C-T

http://identifiers.org/hco/18/GRCh38#46546945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77468200-C-A

46546945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77468200-C-T

46547130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77468013-A-G

46547130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77468013-A-T

46547139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77468005-G-A

46547139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77468005-G-C

http://identifiers.org/hco/18/GRCh38#46547145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77467999-C-A

46547169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77467975-G-T

http://identifiers.org/hco/18/GRCh38#46547194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77467950-C-A

46547194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77467950-C-T

46547356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77467853-G-A

46547429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77467786-G-T

46547620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77467606-G-T

46547661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77467566-G-T

46547784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77467463-G-A

46547878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77467365-T-C

46548084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77467310-C-T

46548219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77467208-C-T

http://identifiers.org/hco/18/GRCh38#46548239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77467187-C-A

46548374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77467075-C-T

46548403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77467054-G-A

46548422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77467036-G-A

46548459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77467004-G-A

46548480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77466983-T-A

46548828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77466657-G-A

46548831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77466654-T-A

46548945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77466539-C-T

http://identifiers.org/hco/18/GRCh38#46549154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77466334-C-A

46553763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77465626-A-G

46553861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77465535-A-G

46554034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77465376-T-C

46554324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77465137-T-C

46554366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77465091-G-C

46554388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77465070-G-T

46554422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77465037-G-C

46554423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77465036-A-G

http://identifiers.org/hco/18/GRCh38#46554597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77464877-A-C

46554660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77464811-G-A

46554712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77464751-G-A

46554715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77464748-G-A

http://identifiers.org/hco/18/GRCh38#46554853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77464593-A-C

46554947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77464493-T-C

46555023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77464409-G-A

46555023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77464409-G-T

46555024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77464408-A-G

http://identifiers.org/hco/18/GRCh38#46555031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77464401-C-A

46555031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77464401-C-G

46555089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77464343-C-T

46555128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 77464305-G-C

46555253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77464194-G-A

46555253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77464194-G-T

http://identifiers.org/hco/18/GRCh38#46555352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77464133-C-A

46555352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77464133-C-G

http://identifiers.org/hco/18/GRCh38#46555416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77464103-A-C

46555416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77464103-A-T

http://identifiers.org/hco/18/GRCh38#46555417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77464102-C-A

http://identifiers.org/hco/18/GRCh38#46555430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77464089-C-A

46555430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77464089-C-T

46555434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77464085-A-G

46555475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77464044-G-A

46555475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77464044-G-C

46555475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77464044-G-T

46555506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77464013-A-G

46555506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77464013-A-T

46555559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77463949-C-T

46555767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77463766-C-T

46555804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77463730-T-C

46555918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77463629-C-T

46556033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77463551-A-G

46556045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77463539-T-A

46556086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77463511-C-T

http://identifiers.org/hco/18/GRCh38#46557235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77462998-C-A

46557241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462992-T-A

46557241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462992-T-C

46557241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462992-T-G

46557254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462979-T-A

46557254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462979-T-C

46557254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462979-T-G

46557341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462905-T-A

46557341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462905-T-G

46557370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: 77462878-C-T

46557379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77462869-A-G

46557492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77462756-G-T

46557515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462732-T-C

46557585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462683-A-G

46557587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462681-G-A

46557587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462681-G-T

46557591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462677-A-G

46557591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462677-A-T

46557593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462675-G-A

46557593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462675-G-T

http://identifiers.org/hco/18/GRCh38#46557602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77462666-C-A

46557602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462666-C-G

46557602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462666-C-T

46557614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462647-G-C

46557614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462647-G-T

46557650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77462608-G-T

46559265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77460901-T-C

46559330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460836-G-C

46559331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460834-A-G

46559331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460834-A-T

46559333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460832-G-A

46559333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460832-G-T

46559335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460830-A-G

46559339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460826-G-C

46559348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460817-C-T

46559351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460814-A-G

46559365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460798-T-A

46559369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460794-C-T

46559384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460776-A-T

46559400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460768-G-C

46559400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460768-G-T

46559404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460764-C-T

46559424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460742-A-T

http://identifiers.org/hco/18/GRCh38#46559430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77460736-C-A

46559430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460736-C-T

46559431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460735-A-T

46559505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77460660-G-A

46559625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460540-T-C

46559625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460540-T-G

46559674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460504-T-C

46559705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460471-T-C

46559720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460457-A-G

46559720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460457-A-T

46559832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460356-A-G

46559854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460334-T-C

46559863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460325-C-T

http://identifiers.org/hco/18/GRCh38#46560013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77460184-C-A

46560013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460184-C-G

46560013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460184-C-T

46560016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460181-G-C

46560016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77460181-G-T

46560111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77460097-C-G

46560298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77459901-T-C

46560304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77459895-T-G

46560406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77459790-T-C

http://identifiers.org/hco/18/GRCh38#46560591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77459605-C-A

http://identifiers.org/hco/18/GRCh38#46560603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77459593-A-C

http://identifiers.org/hco/18/GRCh38#46560689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77459540-C-A

46560689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77459540-C-T

46560721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77459487-G-A

http://identifiers.org/hco/18/GRCh38#46560757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77459440-C-A

46560823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77459357-T-C

46561060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77459104-A-G

46561164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77458974-G-C

46561528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77458427-C-T

46561792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77458165-G-A

46562067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77458077-A-T

46562163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457980-C-T

46562257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457888-G-T

46562337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457807-A-G

46562344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457800-A-T

46562369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457775-G-C

46562456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457679-C-T

http://identifiers.org/hco/18/GRCh38#46562536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77457598-A-C

46562624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457511-C-T

46562712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457433-C-T

46562721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457424-G-A

46562747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457398-A-G

http://identifiers.org/hco/18/GRCh38#46562754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77457387-C-A

46562754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457387-C-T

46562948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457071-G-A

46562950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457069-A-G

http://identifiers.org/hco/18/GRCh38#46562999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77457043-C-A

http://identifiers.org/hco/18/GRCh38#46563000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77457042-C-A

46563000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457042-C-G

46563000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77457042-C-T

46563213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77456829-T-C

46563213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77456829-T-G

46563231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77456812-T-A

46563231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77456812-T-C

46563231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77456812-T-G

http://identifiers.org/hco/18/GRCh38#46563235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77456808-C-A

46563235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77456808-C-T

http://identifiers.org/hco/18/GRCh38#46563298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77456736-C-A

46563298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77456736-C-G

http://identifiers.org/hco/18/GRCh38#46563323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77456711-C-A

46563323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77456711-C-T

46563325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77456709-G-A

46563325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77456709-G-T

http://identifiers.org/hco/18/GRCh38#46563363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77456674-A-C

46563463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77456583-C-T

46563520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77456515-A-T

46566313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77454226-G-C

http://identifiers.org/hco/18/GRCh38#46566462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77454076-C-A

46566462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77454076-C-T

46566480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77454058-G-A

46566480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77454058-G-T

46566484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77454055-C-T

46566503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77454033-T-A

46566503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77454033-T-C

46566503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77454033-T-G

http://identifiers.org/hco/18/GRCh38#46566520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77454016-C-A

46566520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77454016-C-T

46566522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77454014-C-G

http://identifiers.org/hco/18/GRCh38#46566529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77454001-C-A

46566610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453928-C-T

46566635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453904-C-T

46566678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453855-C-G

46566697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453837-C-T

46566714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453820-G-C

46566847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453701-T-C

46566867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453681-T-C

46567005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453566-A-T

46567037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453534-A-G

46567081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453488-G-A

46567150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453426-A-G

http://identifiers.org/hco/18/GRCh38#46567319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77453261-A-C

46567350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453228-T-G

46567363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453215-C-T

http://identifiers.org/hco/18/GRCh38#46567387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77453191-C-A

46567392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453186-T-C

46567513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77453069-C-T

http://identifiers.org/hco/18/GRCh38#46567707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77452906-C-A

46567796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77452822-T-G

46567838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77452799-C-G

http://identifiers.org/hco/18/GRCh38#46567844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77452793-C-A

46567986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77452692-A-G

46568071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77452628-T-G

46568112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77452603-C-G

46568140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77452575-A-G

46568189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77452519-G-A

46568306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77452412-A-G

46568483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77452227-A-G

46568669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77452059-C-G

46568858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77451890-T-A

46569083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77451688-C-T

46569282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77451478-A-G

46569294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77451464-G-T

46569348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77451423-G-T

http://identifiers.org/hco/18/GRCh38#46569440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77451366-A-C

46569509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77451297-T-C

46569533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77451273-T-C

46569542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77451264-G-C

46569542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77451264-G-T

46569545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77451261-T-C

http://identifiers.org/hco/18/GRCh38#46569651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77451155-A-C

46569651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77451155-A-T

http://identifiers.org/hco/18/GRCh38#46569705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77451109-C-A

46569705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77451109-C-G

46569705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77451109-C-T

46569710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77451104-A-G

46569873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77450955-G-T

46569922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77450910-A-G

46569966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77450865-T-C

46570482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77450487-C-G

46570628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77450360-A-G

46570935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77450289-C-T

46571033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77450182-G-C

46571066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77450160-C-G

46571074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77450152-C-T

46571132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77450094-A-G

46571580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449958-A-G

46571679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449893-A-G

46571854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449727-C-G

46571921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449663-C-T

46571978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449607-C-T

46571984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449601-T-C

46572026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449551-G-A

46572026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449551-G-T

http://identifiers.org/hco/18/GRCh38#46572058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77449520-C-A

46572058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449520-C-T

http://identifiers.org/hco/18/GRCh38#46572059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77449519-C-A

46572059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449519-C-T

46572094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77449484-G-A

http://identifiers.org/hco/18/GRCh38#46572124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77449454-C-A

46572124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77449454-C-T

46572179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449399-G-A

46572179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449399-G-T

46572181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449397-A-T

46572195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449380-G-C

46572195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449380-G-T

46572211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449364-C-G

46572211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449364-C-T

46572239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449335-G-A

46572239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449335-G-T

46572258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449316-G-A

46572258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449316-G-T

46572297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449277-T-C

46572465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449092-C-G

46572471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449086-A-G

46572523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449039-G-T

46572540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449022-G-A

46572541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77449021-T-C

46572703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77448900-G-A

46573806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77446431-A-G

46573832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77446416-T-C

46574334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77445950-G-A

46577541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77444763-G-T

http://identifiers.org/hco/18/GRCh38#46577557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77444747-C-A

46577557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77444747-C-T

http://identifiers.org/hco/18/GRCh38#46577572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77444732-C-A

46577572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77444732-C-T

46577618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77444686-G-A

46577618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77444686-G-T

46577686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77444632-C-T

http://identifiers.org/hco/18/GRCh38#46577827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77444493-A-C

46577827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77444493-A-G

http://identifiers.org/hco/18/GRCh38#46578628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77444174-A-C

46579502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77443989-G-A

46579502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77443989-G-T

46579519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77443971-T-C

46579529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77443961-G-A

46579530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77443960-G-C

46579530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77443960-G-T

46579535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77443955-G-T

46579605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77443908-A-G

46579616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77443897-T-C

46579649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77443864-T-C

46579896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77443672-G-T

46580061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77443563-G-T

46585473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77436533-G-A

46585501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77436505-T-C

46585563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77436443-A-G

46586004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77436077-A-T

46586055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77436031-T-G

46586766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77435468-A-T

46587019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77435241-C-G

46587393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77434553-C-T

46587486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77434464-G-A

46587852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77434111-T-C

46587889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77434085-C-T

46587892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77434082-T-A

46587892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77434082-T-C

46588037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77433937-A-T

46588042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77433932-C-G

46588110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77433876-C-T

46588275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77433727-G-T

46588631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77432569-T-A

46588631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77432569-T-C

46588861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77432339-G-A

46588888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77432313-G-A

46590928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77430867-T-A

46590928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77430867-T-C

46590977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77430813-A-G

46591069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77430715-C-G

46591299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77430452-T-C

46591404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77430308-T-C

46591596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77430086-C-T

46591719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77429968-C-T

46591722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77429961-C-T

46591843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77429837-G-T

http://identifiers.org/hco/18/GRCh38#46591924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77429766-A-C

46591924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77429766-A-G

46592040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77429650-T-C

46592124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77429564-C-T

46592130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77429558-G-A

46592143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77429195-T-A

http://identifiers.org/hco/18/GRCh38#46592158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#77429180-A-C

46592196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77429154-G-A

46592196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77429154-G-T

46592228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77429120-T-A

http://identifiers.org/hco/18/GRCh38#46592379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77429005-C-A

http://identifiers.org/hco/18/GRCh38#46592390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77428993-C-A

http://identifiers.org/hco/18/GRCh38#46592653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77428752-C-A

46593192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77428250-G-T

46593218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77428222-A-T

46593264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77428177-T-C

46593414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77428030-C-T

46593547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77427911-G-A

46593547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77427911-G-T

46593549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77427909-C-T

46593643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77427817-G-T

46593712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77427748-C-T

46593805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77427655-A-T

http://identifiers.org/hco/18/GRCh38#46593858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77427603-A-C

46593957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77427509-A-G

46594172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77427316-G-C

46594444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77427158-G-C

46594444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77427158-G-T

46594453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77427149-C-T

46594513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77427088-G-T

46601177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77420546-G-A

46601177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77420546-G-C

46601278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77420448-A-G

46601326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77420400-C-T

46601509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77420220-T-C

46601510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 77420219-G-A

46601578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77420167-C-T

46601607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77420134-T-C

http://identifiers.org/hco/18/GRCh38#46601622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77420125-A-C

46601622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77420125-A-T

http://identifiers.org/hco/18/GRCh38#46601636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77420111-C-A

46601636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77420111-C-G

46601636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77420111-C-T

46601752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77420005-A-G

46603344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77419442-T-C

46603449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77419322-T-G

46603461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77419310-G-A

46603645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77419115-G-A

46603670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77419084-C-T

46603839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77419005-T-G

http://identifiers.org/hco/18/GRCh38#46603878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77418970-C-A

46603906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418948-A-G

46603911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418942-C-T

46603944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418916-G-T

46603948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418912-C-T

46603980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418880-G-A

46604021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418839-A-G

http://identifiers.org/hco/18/GRCh38#46604046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77418817-C-A

46604046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418817-C-G

http://identifiers.org/hco/18/GRCh38#46604077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77418787-A-C

46604077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418787-A-G

46604077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418787-A-T

http://identifiers.org/hco/18/GRCh38#46604144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77418721-A-C

46604299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418572-A-G

46604314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418558-G-T

46604367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418507-T-C

46604463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418423-G-A

46604463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418423-G-T

46604505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418379-A-T

46604534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77418364-G-A

46610626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77417168-A-G

46610626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77417168-A-T

http://identifiers.org/hco/18/GRCh38#46610681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77417113-A-C

http://identifiers.org/hco/18/GRCh38#46610706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77417089-C-A

46610706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77417089-C-T

46610731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77417067-C-G

46610731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77417067-C-T

46610855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77416943-G-A

46610957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77416844-A-G

46611078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77416700-T-G

46611186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77416593-C-T

46611203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77416576-A-G

46611499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77416312-G-T

46611500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77416311-G-T

46611652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77416144-G-T

46611687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77416110-A-G

46611729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77416068-C-T

46611806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77415786-C-T

46612323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77415194-G-C

46612412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77415111-T-C

46612412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77415111-T-G

46612462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77415062-A-T

46612845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77414478-C-T

46612847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77414476-A-G

46612887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77414436-C-T

46615084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77413255-T-G

http://identifiers.org/hco/18/GRCh38#46615274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77413060-C-A

46617451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77410152-C-T

46618109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77409443-C-T

46618130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77409423-G-C

46618130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77409423-G-T

46618209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77409348-C-T

http://identifiers.org/hco/18/GRCh38#46618329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77409229-A-C

46618330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77409228-T-C

46618346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77409212-G-A

46618346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77409212-G-T

46618481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77409094-C-T

http://identifiers.org/hco/18/GRCh38#46618551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77409031-C-A

46618554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77409028-T-A

46618676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77408956-A-G

http://identifiers.org/hco/18/GRCh38#46618738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77408898-C-A

46619122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77408534-A-T

46619339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77408316-T-A

46619339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77408316-T-C

46619357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77408298-G-A

46619461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77408199-G-A

46619506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77408131-C-T

46619530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77408107-C-T

46619753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77407876-G-T

46619812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77407824-C-T

46619881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77407755-A-G

46619921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77407719-C-T

46619968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77407671-G-A

46620102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77407545-T-C

46620102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77407545-T-G

46620579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77406853-T-G

46620690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77406743-T-C

46620715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77406718-C-T

46620883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77406568-C-G

46620883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77406568-C-T

46620907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77406546-C-G

46620907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77406546-C-T

46620918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77406535-C-T

46620919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77406534-T-C

46620976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77406483-A-G

46621065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77406400-G-A

46621217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77406276-G-A

http://identifiers.org/hco/18/GRCh38#46621359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77406135-C-A

46621373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77406092-A-T

46621454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77406007-T-C

46621689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77405526-G-A

46621689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77405526-G-T

46621692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77405523-G-A

46621836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77405375-T-C

46621852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77405359-G-C

46621873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77405339-A-G

46622859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77405089-A-G

46622862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77405086-T-A

46622931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77405032-A-G

46623240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77404807-T-G

46623868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77404228-G-C

46624398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77403753-C-G

46624398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77403753-C-T

46624447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77403725-G-T

46624510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77403689-A-G

46624607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77403645-C-T

46624874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77403462-C-G

46625038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77401625-G-A

46625288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77401418-C-G

46625290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77401416-G-A

46626989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77397717-G-A

46627184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77397526-A-G

46627241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77397487-G-A

http://identifiers.org/hco/18/GRCh38#46627325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77397410-C-A

46627325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77397410-C-G

46627517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77397234-A-G

46627642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77396957-G-A

46627642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77396957-G-T

46627748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77396864-C-T

46627782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77396831-A-G

http://identifiers.org/hco/18/GRCh38#46627808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77396805-C-A

46628022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77396620-G-T

http://identifiers.org/hco/18/GRCh38#46628409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77396234-C-A

46628409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77396234-C-T

46628434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77396209-G-A

46628909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77395452-T-A

46628909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77395452-T-G

46629068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77395329-C-T

46629281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77395166-T-A

46629433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77394977-C-G

46629473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77394932-A-T

46629589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77394810-C-G

46629623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77394776-T-C

46629626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77394773-T-C

46629666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77394748-G-A

46629824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77394623-G-A

46629825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77394622-A-G

46629825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77394622-A-T

46630024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77394454-C-T

46630220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77394258-C-G

46630250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77394228-C-T

46630303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77394175-G-A

46630335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77394143-T-C

46630357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, undefined
orthologous variants: 77394127-A-G

46630776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77393333-G-A

46630776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77393333-G-C

46630776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77393333-G-T

46630889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77393239-G-A

46630909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77393219-G-A

46632604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77392625-G-C

http://identifiers.org/hco/18/GRCh38#46632703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77392528-C-A

http://identifiers.org/hco/18/GRCh38#46632750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77392481-A-C

46632811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, undefined
orthologous variants: 77392420-G-A

46633228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77392011-T-C

46633761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77391832-A-G

46634174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77391404-A-T

46634887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77390913-G-T

46635174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77390721-A-G

46635227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77390673-C-G

46635375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77390482-G-A

46635407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77390449-C-G

46635407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77390449-C-T

46635617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77390164-G-A

46635664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77390117-G-A

46635729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77390049-A-G

46636254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77389135-G-T

46636629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77386369-T-C

46636630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77386360-C-T

46636684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77386308-T-G

46639490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77383706-A-G

http://identifiers.org/hco/18/GRCh38#46639508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77383698-C-A

46639544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77383665-G-T

46639569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77383658-C-T

46639579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77383648-A-T

http://identifiers.org/hco/18/GRCh38#46639669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77383558-C-A

46639669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77383558-C-T

46639723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77383504-T-A

http://identifiers.org/hco/18/GRCh38#46639823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77383403-C-A

46639823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77383403-C-T

46639840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77383387-C-T

46639859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77383368-A-G

46639875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77383353-A-G

46639883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77383345-T-A

46639883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77383345-T-G

46640109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77383175-C-T

http://identifiers.org/hco/18/GRCh38#46640308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77382967-C-A

46640357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77382921-C-G

46640358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77382920-C-T

46640784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77382069-T-C

46640943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77381923-C-T

http://identifiers.org/hco/18/GRCh38#46640948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77381918-C-A

46640948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77381918-C-T

46640978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77381888-C-G

46640995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77381866-A-T

46641114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77381744-C-T

46641122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77381720-C-T

46641415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77381469-A-T

46641776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77381149-T-A

46641776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77381149-T-G

http://identifiers.org/hco/18/GRCh38#46641836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77381088-C-A

46641836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77381088-C-T

46641893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77381047-T-C

46641925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77381031-C-T

http://identifiers.org/hco/18/GRCh38#46641995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77380969-C-A

46641995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77380969-C-G

46641995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77380969-C-T

http://identifiers.org/hco/18/GRCh38#46642001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77380963-A-C

46642019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77380945-T-C

http://identifiers.org/hco/18/GRCh38#46642099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77380868-C-A

46642130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77380839-A-G

46642130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77380839-A-T

46642410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77380581-G-A

46642571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77380422-C-G

46642636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77380367-G-T

http://identifiers.org/hco/18/GRCh38#46642752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77380254-A-C

46642752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77380254-A-G

46642827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77380179-C-T

46642913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77380105-C-T

46643077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77379563-C-T

46643302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77379291-C-T

46643359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77379246-G-T

46643583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77379073-C-T

46643731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77378924-G-A

46644241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77378447-A-G

46645045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77378094-A-G

46645374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77377763-C-G

46645374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77377763-C-T

46645558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77377562-T-C

46645642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77377477-G-T

46645759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77377386-A-T

46645765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77377380-T-C

46645844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77377327-A-T

46646085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77377091-G-A

http://identifiers.org/hco/18/GRCh38#46646464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77376615-A-C

46646722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77376404-G-A

46646722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77376404-G-T

46646793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77376336-G-T

http://identifiers.org/hco/18/GRCh38#46646810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77376319-C-A

46646810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77376319-C-T

46646839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77376291-G-A

46646839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77376291-G-C

46646841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77376289-C-T

46646936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77376215-G-A

46647076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77376133-T-A

46647278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77375942-C-T

46647773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77375454-G-T

46647936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77375225-G-C

46648464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374941-T-C

46648577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374824-C-T

http://identifiers.org/hco/18/GRCh38#46648582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77374819-A-C

46648830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374551-A-G

46648907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374469-G-A

46648907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374469-G-T

46648961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374374-G-A

46649007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374318-G-A

46649007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374318-G-C

46649007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374318-G-T

http://identifiers.org/hco/18/GRCh38#46649020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77374308-C-A

46649047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374280-G-T

46649051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374276-T-C

46649051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374276-T-G

46649079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374248-G-A

46649079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374248-G-T

46649117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374210-A-G

http://identifiers.org/hco/18/GRCh38#46649131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77374196-C-A

46649182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77374146-A-G

46649283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77374044-G-A

46649495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77373908-T-C

46649728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77373640-G-A

46650012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77373247-T-G

46650112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77373146-G-A

http://identifiers.org/hco/18/GRCh38#46650198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77373062-C-A

46650273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77372990-G-T

46650541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77372719-C-T

46650740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77372534-G-A

46650797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77372470-T-G

46650984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77372297-T-A

46651558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77371758-G-A

46651587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77371737-A-G

46651826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77371495-T-C

46651870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77371469-G-A

46651911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77371427-G-C

46651955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77371386-T-C

46652015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77371328-G-A

46652015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77371328-G-T

46652042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77371322-T-A

46652042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77371322-T-C

46652146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77371239-T-C

46652265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77371125-T-C

46652548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77370884-G-T

46652567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77370865-G-A

46652594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77370839-C-T

46652608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77370816-T-C

http://identifiers.org/hco/18/GRCh38#46652618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77370806-C-A

http://identifiers.org/hco/18/GRCh38#46652861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77370588-C-A

46652888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77370560-T-C

46653050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: 77370432-C-G

http://identifiers.org/hco/18/GRCh38#46653058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77370424-C-A

http://identifiers.org/hco/18/GRCh38#46656896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77369815-C-A

46656987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77369698-A-G

46657008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: missense variant
orthologous variants: 77369677-C-G

46657051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5 prime UTR variant
orthologous variants: 77369634-C-T

46657054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5 prime UTR variant
orthologous variants: 77369631-A-G

46657054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5 prime UTR variant
orthologous variants: 77369631-A-T

46657069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5 prime UTR variant
orthologous variants: 77369616-A-G

http://identifiers.org/hco/18/GRCh38#46657097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77369587-A-C

46657097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5 prime UTR variant
orthologous variants: 77369587-A-G

46657119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5 prime UTR variant
orthologous variants: 77369565-T-C

http://identifiers.org/hco/18/GRCh38#46657130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77369554-C-A

46657130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5 prime UTR variant
orthologous variants: 77369554-C-T

46657179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5 prime UTR variant
orthologous variants: 77369510-T-C

46657213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26521
most severe consequence: 5 prime UTR variant
orthologous variants: 77369475-C-T