73254725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85446590-C-T

73254782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85446643-C-G

73254782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85446643-C-T

http://identifiers.org/hco/2/GRCh38#73254932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85446790-C-A

73254932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85446790-C-T

73254938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85446796-T-A

73254938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85446796-T-C

73255156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85446928-A-G

73255179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85446951-G-A

73255532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85447251-G-T

http://identifiers.org/hco/2/GRCh38#73255713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85447405-C-A

73255919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85447559-G-A

73255919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85447559-G-T

73256069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85447664-G-T

73256224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85447821-G-T

http://identifiers.org/hco/2/GRCh38#73256574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85448108-C-A

73257097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85448472-T-C

73257237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85448602-G-T

73257247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85448612-T-C

73257322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85448681-A-G

73257416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85448759-T-C

73257424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85448767-A-G

http://identifiers.org/hco/2/GRCh38#73257427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85448770-C-A

73257427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85448770-C-T

73257445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85448786-G-A

73257445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85448786-G-T

73257585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85448872-A-G

73257655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85448938-G-A

73257660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85448941-A-G

73257894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85449105-T-C

http://identifiers.org/hco/2/GRCh38#73257929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85449139-C-A

http://identifiers.org/hco/2/GRCh38#73257935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85449142-C-A

http://identifiers.org/hco/2/GRCh38#73257946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85449152-C-A

73257961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85449159-A-G

73258020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85449207-T-C

73258020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85449207-T-G

73258064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85449228-G-A

73258071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85449235-C-T

73258230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85449351-G-A

73258230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85449351-G-T

73258234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85449355-G-A

73258234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85449355-G-T

http://identifiers.org/hco/2/GRCh38#73258427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85449512-C-A

73258596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85449645-G-T

73258647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85449678-G-A

73258647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85449678-G-T

73258678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 3 prime UTR variant
orthologous variants: 85449709-T-C

73259166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85450167-G-A

73259166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85450167-G-C

73259299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 85450301-G-A

73259303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 85450305-A-G

73259340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85450337-G-A

73259340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85450337-G-T

73259403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85450401-G-A

73259403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85450401-G-C

73259403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85450401-G-T

73259413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85450405-G-A

73259413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85450405-G-T

73259439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85450420-G-A

73259581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85450544-G-C

73259784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85450733-G-A

73260364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, undefined
orthologous variants: 85452036-T-C

73260378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85452051-C-G

73260378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85452051-C-T

73260648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85452286-G-A

73260648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85452286-G-T

http://identifiers.org/hco/2/GRCh38#73260660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85452298-C-A

73260660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85452298-C-T

73260663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85452301-T-C

73260710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85452348-C-T

73260712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85452350-C-T

73260798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous_variant, undefined
orthologous variants: 85452434-G-A

73260798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: missense_variant, undefined
orthologous variants: 85452434-G-T

73260828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85452464-G-A

73260828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: stop gained
orthologous variants: 85452464-G-T

73261069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85452719-T-G

73261082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85452743-G-A

73261288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85453058-G-A

73261321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85453091-G-A

73261862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85453521-T-G

73263064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85454444-G-A

73263064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85454444-G-T

73263146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85454485-A-G

73263188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85454527-A-G

73263227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85454564-T-C

http://identifiers.org/hco/2/GRCh38#73263281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85454618-C-A

73263281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85454618-C-T

http://identifiers.org/hco/2/GRCh38#73263290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85454627-C-A

73263290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85454627-C-T

http://identifiers.org/hco/2/GRCh38#73263320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85454658-C-A

73263320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85454658-C-T

http://identifiers.org/hco/2/GRCh38#73263445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85454674-C-A

73263445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85454674-C-T

http://identifiers.org/hco/2/GRCh38#73263450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85454679-C-A

73263644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85454803-G-C

73263646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85454805-G-A

73263646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85454805-G-T

73263650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85454809-A-G

73263653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85454812-C-G

73263668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85454828-G-A

73263668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85454828-G-T

73263844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85455005-A-G

http://identifiers.org/hco/2/GRCh38#73263955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85455105-C-A

73263955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: missense variant
orthologous variants: 85455105-C-G

73263955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85455105-C-T

73263988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85455138-G-A

73264311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: missense variant
orthologous variants: 85455416-C-G

73264311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85455416-C-T

73264314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85455419-T-C

73264534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85455639-G-A

73264534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85455639-G-T

73264630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85455738-G-T

73264697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85455805-A-G

73264905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85456300-T-C

http://identifiers.org/hco/2/GRCh38#73265077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85456441-C-A

73265077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85456441-C-G

73265077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85456441-C-T

73265169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85456507-G-T

http://identifiers.org/hco/2/GRCh38#73265256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85456566-C-A

73265256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85456566-C-G

73265256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85456566-C-T

73265283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 85456611-T-A

http://identifiers.org/hco/2/GRCh38#73265340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85456668-C-A

73265340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85456668-C-T

http://identifiers.org/hco/2/GRCh38#73265361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85456689-C-A

73265385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85456713-G-A

73265406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: missense variant
orthologous variants: 85456734-C-G

73265406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85456734-C-T

http://identifiers.org/hco/2/GRCh38#73265574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85456902-C-A

73265574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85456902-C-T

73265663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85456993-G-A

73265663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85456993-G-C

73265663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85456993-G-T

http://identifiers.org/hco/2/GRCh38#73265681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85457011-C-A

73265681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85457011-C-T

73265774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85457088-G-A

73265774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85457088-G-T

http://identifiers.org/hco/2/GRCh38#73265783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85457095-C-A

73265783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85457095-C-T

73265793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85457106-G-A

http://identifiers.org/hco/2/GRCh38#73265992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85457300-A-C

73266172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85457478-C-T

73266202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85457508-C-G

73266217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85457520-G-A

73266286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85457580-G-A

73266341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85457644-A-G

http://identifiers.org/hco/2/GRCh38#73266358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85457658-C-A

73266358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85457658-C-T

73266408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85457698-T-C

73266408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85457698-T-G

73266413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85457703-G-A

73266413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85457703-G-T

http://identifiers.org/hco/2/GRCh38#73266450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85457742-C-A

73266450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 85457742-C-T

73266514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85457806-C-T

73266571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85457863-G-A

73266571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85457863-G-C

http://identifiers.org/hco/2/GRCh38#73266666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85457958-C-A

73266666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 85457958-C-T

73266667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85457959-G-A

73266667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85457959-G-T

73266685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 85457977-G-A

73266685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 85457977-G-C

73266685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 85457977-G-T

http://identifiers.org/hco/2/GRCh38#73266735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85458027-C-A

73266735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85458027-C-T

73266811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85458101-G-T

73266826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85458106-G-T

73266831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85458111-G-A

73266831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85458111-G-T

73267126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85458995-C-T

73267498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85459331-C-T

73267524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85459348-T-C

http://identifiers.org/hco/2/GRCh38#73268646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85460737-C-A

73268646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85460737-C-G

73268646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85460737-C-T

73268707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85460789-G-A

73268707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85460789-G-C

73268707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron variant
orthologous variants: 85460789-G-T

73268877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: missense variant
orthologous variants: 85460959-G-A

73268877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: missense variant
orthologous variants: 85460959-G-C

73268877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85460959-G-T

73268933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: missense_variant, undefined
orthologous variants: 85461015-T-A

73268933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: missense_variant, undefined
orthologous variants: 85461015-T-C

73269016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85461098-G-T

73269100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85461182-G-A

73269100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85461182-G-C

73269100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85461182-G-T

73269166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85461248-C-T

73269199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85461281-G-C

73269199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85461281-G-T

http://identifiers.org/hco/2/GRCh38#73269226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85461302-C-A

73269226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85461302-C-T

73269259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85461335-G-A

73269259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85461335-G-C

73269388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous variant
orthologous variants: 85461464-T-C

http://identifiers.org/hco/2/GRCh38#73269610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#85461686-C-A

73269610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous_variant, undefined
orthologous variants: 85461686-C-G

73269610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: synonymous_variant, undefined
orthologous variants: 85461686-C-T

73269737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 85461814-G-A

73269737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 85461814-G-T

73269767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 85461844-G-T

73269809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85461886-G-A

http://identifiers.org/hco/2/GRCh38#73269845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#85461924-C-A

73269845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85461924-C-T

73269878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85461966-G-A

73269878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85461966-G-T

73270189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85462934-A-G

http://identifiers.org/hco/2/GRCh38#73270399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85463170-C-A

73270624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85463347-C-T

http://identifiers.org/hco/2/GRCh38#73270729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85463437-C-A

73270729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85463437-C-T

http://identifiers.org/hco/2/GRCh38#73270737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85463445-C-A

http://identifiers.org/hco/2/GRCh38#73272199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85465351-A-C

73272311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85465449-A-T

73272447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85465562-G-T

73272451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85465566-G-A

73272451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85465566-G-T

73272459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85465574-G-A

73273026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85466134-G-T

http://identifiers.org/hco/2/GRCh38#73273069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85466178-C-A

73273069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85466178-C-G

73273581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85466484-C-T

73273915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85467463-G-A

73274337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85467977-A-G

73276969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85470728-G-C

73277112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85470839-G-C

73277118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85470845-G-T

73277119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85470846-G-C

73277119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85470846-G-T

73277284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85470986-G-C

73277391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85471631-T-C

73277517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85471747-C-T

73277938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85472169-G-A

73278120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85472350-G-C

73278120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85472350-G-T

http://identifiers.org/hco/2/GRCh38#73280442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85476419-C-A

73280493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85476466-C-T

73280494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85476467-G-A

73280494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85476467-G-T

73280746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85476729-G-A

http://identifiers.org/hco/2/GRCh38#73280942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85477151-C-A

73280987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 85477194-A-G

73281244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85477367-A-T

http://identifiers.org/hco/2/GRCh38#73281366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85477477-C-A

73281380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85477497-A-G

73281548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85477653-C-G

73281702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85477781-G-C

73281942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85478142-G-A

73281946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85478146-C-T

73282853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85478407-A-G

73283361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85478907-G-A

73283431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85478972-C-G

http://identifiers.org/hco/2/GRCh38#73283926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85479454-A-C

73284044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85479575-G-A

73284044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85479575-G-T

73284046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85479576-G-A

73284046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85479576-G-T

73284434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29409
most severe consequence: 5 prime UTR variant
orthologous variants: 85479953-G-A